3M Steri Vac Site and Installation Guide

3M™ Steri-Vac™ Sterilizer/Aerator GS Series
Site Planning
& Installation Guide
3M
Site Planning and Installation Guide
Table of Contents
I. Introduction 3 VI: Install Guide for 3M™ In-Wall Mounting Unit 30
Device Safety Compliance ..............................................................................3 General Information ..................................................................................... 30
EMC Compliance............................................................................................4 General Specifications ................................................................................. 30
Plan and Install ...............................................................................................5 Finished Installation ..................................................................................... 30
Finished Wall Specifications ..........................................................................31
II. Select the Equipment 6
Floor Preparation ..........................................................................................31
III. Select the Location 9 Installing Permanent Floor Channels ..............................................................31
Site Planning Worksheet ............................................................................... 11 Placement of 3M™ Steri-Vac™ Sterilizer/Aerators onto the Stacking Rack.........32
Proposed Location of Equipment ................................................................... 12 Access Area ...............................................................................................32
Pre-Installation Visit and Site Readiness Verification ...................................... 14 Installation of Stainless Steel Panels .............................................................32
Stop and Hook Adjustment .......................................................................... 33
IV. Preparing the Area and Service Requirements 15
Flexible Connections .................................................................................... 33
Preparing the Selected Area.......................................................................... 15
Installing the Louvered Panel ....................................................................... 33
Utilities ......................................................................................................... 15
Figure References for Section VI................................................................... 34
Electrical Service Requirements ....................................................................16
Compressed Air Requirements...................................................................... 17 Notes 43
Compressor System ..................................................................................... 17
ANNEX A Symbols, Safety Warnings and Cautions 44
Filters .......................................................................................................... 18
Document Conventions................................................................................ 44
Multiple Sterilizer/Aerator Installations ........................................................... 18
3M™ Steri-Vac™ Sterilizer/Aerator GS Series – Explanation of Product and
Compressed Air Line Installation Kit............................................................... 18 Packaging Label and Symbols ..................................................................... 44
Compressor Location ................................................................................... 18 3M™ Steri-Gas™ EO Gas Cartridges – Explanation of Label and Symbols ......... 44
Ethylene Oxide Vent Line Requirements ......................................................... 19 Danger........................................................................................................ 44
3M™ Abator (Emission Control Devices) ........................................................19 First Aid ...................................................................................................... 45
Vent Line Labeling and Install Considerations ................................................ 20 Dangers ...................................................................................................... 45
Local Exhaust Hood Requirements ............................................................... 22 Warnings .................................................................................................... 45
Exhaust Ventilation System Planning and Design........................................... 22 Cautions ..................................................................................................... 45
Exhaust Ventilation System Specifications .................................................... 23
Ductwork .................................................................................................... 23 ANNEX B Worksheets 46
Exhaust Fan ................................................................................................ 23 Site Planning Worksheet .............................................................................. 46
Ventilation Failure Detector........................................................................... 23 Equipment Location Worksheet .....................................................................47
First Aid: Exposure to Ethylene Oxide (EO) .....................................................25 ANNEX C Site Readiness and Installation Verification Forms 48
Ethylene Oxide Storage .................................................................................25 Site Readiness Verification Form ................................................................. 48
Requirements for a Vented Cabinet............................................................... 26 Installation Verification Form ........................................................................ 49
Connect EO Storage Cabinet to GS Series Sterilizer Dedicated Exhaust ......... 26
Disposal of 3M™ Steri-Gas™ EO Gas Cartridges ..............................................27 ANNEX D 3M™ Steri-Gas™ EO Gas Cartridge Dilution Charts 50
Outside Discharge ........................................................................................27
ANNEX E Bibliography and Compliance References 51
V. Final Installation and Support 28 Equipment and Ethylene Oxide (EO) Compliance Documents ..........................51
Site Readiness Verification ...........................................................................28
ANNEX F Disposal of Packaging 51
Unpacking the GS Series Sterilizer .................................................................28
Contact Information ......................................................................................52
System Checkout and In-Service Training ..................................................... 29
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I. Introduction
This Site Planning and Installation Guide is intended to provide information for prospective and new
purchasers of the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series, in order to help plan for and execute
site and installation requirements.
The purchaser is responsible for providing required GS Series sterilizer service requirements to the
area where the equipment will be installed. These services include electricity, compressed air,
and an ethylene oxide (EO) vent line. A dedicated exhaust system is required for installing the
3M™ Steri-Vac™ Exhaust Hood option.
The purchaser is responsible for installing the GS Series sterilizer and accessory equipment
in their permanent location and to connect the required services to the unit(s). The purchaser
is also responsible for ensuring that all national, state and local code requirements are met
(e.g., EO abatement, state of California seismic bracing, etc.). At the time of installation, 3M Health
Care service personnel or authorized 3M service personnel will require written documentation to
verify the requirements for room ventilation and non-recirculating ventilations systems are met.
See ANNEX A for a complete listing of symbols, safety warnings and cautions.
Device Safety Compliance

The 3M™ Steri-Vac™ Sterilizer/Aerator GS Series is an instrument and Class II medical device per the
CAUTION U.S. Food and Drug Administration (FDA) classification definitions. It is a Class IIb medical device per
To reduce the risk of injury, always follow the the European Union Medical Device Directive (MDD) and carries a CE mark related to the Medical
procedures described in this Site Planning and Device Directive 93/42/EEC as confirmed in the Declaration of Conformity.
Installation Guide.
The 3M™ Steri-Vac™ Sterilizer/Aerator GS Series is listed as Laboratory Electrical Equipment for Use
in Health Care Applications and carries the UL mark with adjacent indicators “C” and “US” based on
compliance to the standards UL 61010-1 and CAN/CSA 22.2 No. 61010-1.
The 3M™ Steri-Vac™ Sterilizer/Aerator GS Series is designed, manufactured, and tested to meet
the safety and performance requirement of common safety codes and standards which include
applicable portions of the following standards demonstrated by the CB Scheme Certificate and
test report issued by Underwriters Laboratories (UL):
• IEC/EN 61010-1. Safety requirements for electrical equipment for measurement, control, and
laboratory use - Part 1: General requirements.
• IEC/EN 61010-2-010. Safety requirements for electrical equipment for measurement, control
and laboratory use - Part 2-010: Particular requirements for laboratory equipment for the heating
of materials.
• IEC/EN 61010-2-040. Safety requirements for electrical equipment for measurement, control,
and laboratory use - Part 2-040: Particular requirements for Sterilizer/Aerators and washer
disinfectors used to treat medical devices.
• RoHS Directive, Directive 2011/65/EU of the European Parliament and of the Council on the
restriction of the use of certain hazardous substances in electrical and electronic equipment.
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I. Introduction (continued)
EMC Compliance
The 3M™ Steri-Vac™ Sterilizer/Aerator GS Series complies with the following EMC standards as
Note: This equipment has been tested and found confirmed in the Certificate of Compliance generated by 3M:
to comply with the limits for a Class A digital device,
• IEC 61326-1. Electrical equipment for measurement, control and laboratory use - EMC requirements
pursuant to Part 15 of the FCC Rules. These limits are
- Part 1: General requirements.
designed to provide a reasonable protection against
harmful interference when the equipment is operated • EMC requirements of the CE mark EMC Directive 2004/108/EC.
in a commercial environment. This equipment
• Australian EMC requirements as confirmed in the Supplier’s Declaration of Conformity that is linked
generates and can radiate radio frequency energy
to the RCM Mark.
and, if not installed and used in accordance with this
document and the 3M™ Steri-Vac™ Sterilizer/Aerator • As a Class A digital apparatus meeting all requirements of the Canadian Interference-Causing
GS Series Operator Manual, may cause harmful Equipment Regulations.
interference to radio communications. Operation of
See ANNEX E for a complete list of related compliance standards for the 3M™ Steri-Vac™
this equipment in a residential area is likely to cause
Sterilizer/Aerator GS Series.
harmful interference in which case the purchaser
will be required to correct the interference at their
own expense. In addition, operation of this device
may accept any interference received, including
interference that may cause undesired operation.
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I. Introduction (continued)
Plan and Install
The following describes the tasks for planning and preparing for a successful installation. While each
Site planning is a critical aspect for a successful installation site is unique, the following steps are common to all situations:
installation process. Site planning includes
considerations for: the location, the work flow, Step 1 Select the Equipment
the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series 3M offers a complete system of products for ethylene oxide (EO) sterilization, including two sizes of
service requirements, 3M™ Steri-Gas™ EO Gas 3M™ Steri-Vac™ Sterilizer/Aerator GS Series. Both sizes are available in single door or double door
Cartridge storage requirements both near the GS configurations. Use the 3M™ Abator, where applicable, for efficient abatement of exhausted EO and for
Series sterilizer and storage for larger volumes, any using supporting accessory equipment. Selecting the size, quantity and configuration of the GS Series
connected hardware such as the 3M™ Abator, sterilizer and the number of 3M™ Abators is the first equipment selection task. Second, select any
3M™ Stacking Rack 1237, ventilation apparatuses, required auxiliary equipment. Additional detailed equipment technical specification information for the
and local code requirements. The purchaser must products is available from 3M. Use Table 1 on the following page to document selected equipment.
comply with all state and local regulations affecting
the use of ethylene oxide (EO). It is important
to have a properly planned and acceptably
Step 2 Select a Location
prepared site to ensure the GS Series sterilizer Step 2 recommends a process for analyzing a site and for selecting a suitable location for installing the
operates safely and effectively. All site planning Sterilizer/Aerator system. This Guide includes sample proposed site plans, with architectural details,
and preparation must be completed prior to the for a satisfactory site design. It also includes information on how to design the site. Site Planning and
scheduled installation date. Equipment Location Worksheets are provided in ANNEX B.
Step 3 Prepare the Area and Service Requirements

Critical service requirements must be met before completing and approving the 3M™ Steri-Vac™
Sterilizer/Aerator GS Series Site Readiness Verification Form. These requirements include acceptable
room ventilation, connections to electrical power, connections to vent lines, and compressed air lines.
Service requirements are detailed in Section III.
The purchaser is responsible for securing and scheduling all contracted services in order to meet
installation requirements and for supplying details of the service requirements to the contractors.
The final installation support visit will not be scheduled until all equipment installation requirements
have been met, verified, and documented on the Site Readiness Verification Form found in ANNEX C.
Sections II and III provide information detailing service specifications and requirements. ANNEX B
provides Site Planning and Equipment Location Worksheets. This information can be reproduced
and provided to service contractors, as necessary, to complete the required pre-installation work.
Deviations from the Site Plan:
The purchaser should document any deviations from the recommended 3M Site Planning guidance
and communicate the deviations to 3M Health Care service personnel or authorized 3M service
personnel prior to installation.
Step 4 Install the Equipment

Final equipment hook-up and installation support is performed by 3M Health Care service personnel
or authorized 3M service personnel. A final Installation Verification Form is completed at the end of
equipment installation.
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II. Select the Equipment

Table 1 provides the complete listing of 3M™ Steri-Vac™ Sterilizer/Aerator GS Series products and
accessories equipment. This Table provides product descriptions, dimensions and other information
that is important to consider in equipment selection. 3M Sales and Service personnel will consult and
assist in selecting the appropriate equipment in order to meet specific facility and use requirements.
See Figure 1 for GS5 dimensions and elevations. See Figure 2 for GS8 dimensions and elevations.
Table 1 – 3M™ Steri-Vac™ Product and Accessory Options
Exterior
Quantity
Chamber Size
Select
Product Description Shipping Operational Dimensions
Weight Weight
Area H×W×D H×W×D
Factors to consider in 3M Steri-Vac 163 kg 127 kg
™ ™
Single Door – EO
Sterilizer/Aerator (359 lbs) (281 lbs)
equipment selection: GS5 Sterilizer/Aerator Single Door Single Door 136 L 38 × 43 × 83 cm 70.9
× 76.2 × 95.0 cm
(4.8 cubic (15 × 17 × 32.5 in)
• Chamber size related to processing volume feet) (27.9 × 30.0 × 37.4 in)
3M Steri-Vac
™ ™
169 kg 132 kg
Double Door – EO
requirements, including future volume Sterilizer/Aerator (373 lbs) (290 lbs)
Sterilizer/Aerator
GS5 Double Door Double Door
requirements
3M™ Steri-Vac™ 355 kg 261 kg
• Single door or double door configuration based Sterilizer/Aerator Single Door – EO (782 lbs) (576 lbs)
Sterilizer/Aerator
on process flow and available space GS8 Single Door Single Door 223 L 46 × 51 × 97 cm 179.8 × 94.0 × 109.0 cm
(7.9 cubic (18 × 20 × 38 in) (70.8 × 37.0 × 42.9 in)
• National, state, and local requirements for 3M™ Steri-Vac™ Double Door – EO 362 kg 267 kg feet)
Sterilizer/Aerator (799 lbs) (593 lbs)
ethylene oxide (EO) abatement as applicable GS8 Sterilizer/Aerator Double Door Double Door
• 3M™ Steri-Vac™ EO Gas Cartridge type, volume
3M™ Abator
and storage requirements. A vented liquid Emission 212 kg 163 kg 80.0 cm × 82.0 × 105.0 cm
Models 50, 50AN, NA
Control System (469 lbs) (360 lbs) (31.0 × 32.0 × 41.0 in)
50AE
flammable storage cabinet is required for
EO gas storage. See Section III for additional 3M™ Steri-Vac XL 147 kg 115 kg
Single Door
information. Aerator (outside U.S. (325 lbs) (253 lbs)
Aerator
only for health care) Single Door Single Door 141.5 L
(4.5 cubic 38 × 43 × 83 cm 61.0 x 77.0 x 89.0 cm
3M Steri-Vac XL
™
156 kg 124 kg feet) (15 × 17 × 32.5 in) (24.0 x 30.3 x 35.0 in)
Double Door
Aerator (outside U.S. (345 lbs) (273 lbs)
Aerator
only for health care) Double Door Double Door
Quantity
Select
Product Part Number Description Dimensions
H×W×D
78-8055-6040-2 Stainless lower basket 39 × 80 × 18 cm (15.5 × 31.5 × 7 in)

Extra Baskets
GS5 and XL Aerator
78-8055-6039-4 Stainless upper basket 39 × 80 × 18 cm (15.5 × 31.5 × 7 in)
78-8078-8313-3 Stainless steel lower basket 47 × 95 × 20 cm (18.5 × 37.5 × 8 in)
Extra Baskets 78-8078-5399-5 Stainless steel upper half basket 47 × 47 × 20 cm (18.5 × 18.5 × 8 in)
GS8
78-8078-6251-7 Stainless steel basket cover Cover fits on top of lower basket
Note: Equipment may vary in overall exterior dimensions if accessories (e.g. exhaust duct, leveling
feet) are added.
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Figure 1. 3M™ Steri-Vac™ Sterilizer/Aerator GS Series, Model GS5

Single Door Dimensions
95 cm
76.2 cm (37.4 in.)
30.5 cm (30 in.)
(12 in.)
50.2 cm
(19.8 in.)
70.9 cm
(27.9 in.)
47.6 cm
7.6 cm (18.75 in.) 52 cm
(3 in.) (20.5 in.)
26.6 cm
(10.5 in.)
44.2 cm
(17.4 in.)
7.6 cm
(3 in.)
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Figure 2. 3M™ Steri-Vac™ Sterilizer/Aerator GS Series, Model GS8 Single Door

Dimensions and Elevations
94.0 cm 109.2 cm
(37 in.) (42.9 in.)
72.4 cm
(28.5 in.)
61.0 cm
(24 in.) Plan View
Unload Side
66 cm
(26 in.)
31.8 cm
(12.5 in.)
54.6 cm
(21.5 in.) 179.8 cm 92.7 cm
(70.8 in.) (36.5 in.)
88.9 cm From 54.6 cm
(35 in.) Ground (21.5 in.)
7.6 cm
(3 in.)
Load Side
109.2 cm
(43 in.)
3.2 cm
(1.25 in.)
Unload Side clearance
(two door) between floor
and bottom
Power of Side and
Compressed Air Front Panels
Vent Line
Side Elevation Front Elevation
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III. Select the Location

Give careful consideration in selecting the location for the 3M™ Steri-Vac™ Sterilizer/Aerator GS
Series and accessories in order to ensure that facility, compliance, and safety requirements are met.
This section provides information on requirements that the equipment location must meet related to
Recommended Environmental Operating Specifications (Table 2), occupational safety, and work flow
aspects. Prior to installation, 3M Health Care service personnel or authorized 3M service personnel
will request written verification that the requirements for the general room ventilation rate and the
non-recirculating ventilation system, as described in this Guide and documented on the Site Readiness
WARNING Verification Form, are met (see ANNEX C). At the time of installation, 3M Health Care service
personnel or authorized 3M service personnel will require the purchaser's requirements document and
To reduce the risk of shock due to
hazardous voltage, do not operate the
verification in writing stating that the requirements for general room ventilation rate, non-recirculation,
3M™ Steri-Vac™ Sterilizer/Aerator GS Series and dedicated system requirements are met.
outside the environmental conditions as
stated in this Guide. Table 2 – Recommended Environmental Operating Specifications
Environmental Condition Condition Range Units

DANGER Altitude 2500 (max) Meters
Operating Temperature* 15–35 °C
To reduce the risks associated with
exposure to ethylene oxide: Humidity 20–80 (non-condensing) % RH
Voltage Range (Frequency)
Ensure a minimum of ten (10) air exchanges 200–240 (50/60) VAC (Hz)
Single Phase
per hour (ACHs) for the room in which the
3M™ Steri-Vac™ Sterilizer/Aerator GS Series Current: GS5 7 A
is installed. GS8 12 A
Do not operate the 3M™ Steri-Vac™ Sterilizer/ Transient Over Voltages Category II N/A
Aerator GS Series outside the environmental Pollution Degree 2 N/A
conditions as stated in this Guide.
Ensure the instructions detailed in this * Operating the 3M ™
Steri-Vac™ Sterilizer/Aerator GS Series in a temperature environment that is close to the sterilization
Guide are followed when planning the process temperature set point (e.g. 35ºC operating environment and a 38ºC sterilization process temperature set point)
ventilation system. may result in a temperature fault during the sterilization process.
Note: Verify the requirements and follow all applicable national, state, and local environmental
regulations concerning proper installation of the GS Series sterilizer and any 3M™ Abator for control
of ethylene oxide (EO) emissions. It is important to place the sterilizer in a contained area, with traffic
routed around or away from the area, and restricted personnel access. The size of the area should
be 30 m3 (1000 ft3), or more, and have a minimum of 10 air exchanges per hour. Do not place the
sterilizer or 3M™ Steri-Gas™ EO Gas Cartridges in an area of possible ignition sources.
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An appropriate selected location must meet all of the following requirements. The location:
• has no flammable gases other than ethylene oxide (EO) present at the location.
• is not a high traffic area.
• is well-ventilated with at least 10 air changes per hour. The flow of air is away from the equipment
operator (Figure 3). Recommended room size is a minimum of 28.32 m3 (1,000 ft3).
• has a non-recirculating ventilation system. The exhaust hood, if used, must be connected to an
exhaust system that is dedicated to the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series area and
supplies air flow >125 cubic feet per minute (CFM) through each vent hood.
• allows 51 cm (20 inches) of clearance space at the top, rear, and sides of the GS Series sterilizer
for maintenance and service (Figure 5).
• provides a suitable location for storage of 3M™ Steri-Gas™ EO Gas Cartridges that includes a
flammable liquids cabinet vented to the outside.
Appropriate installation of the air handling system is important and should be designed and installed
to provide air flow through the entire room and direct air movement away from the GS Series sterilizer
and Operator as shown in Figure 3.
Figure 3. Example of Acceptable and Unacceptable Air Flow
Acceptable Air Flow Unacceptable Air Flow
or Exhaust Exhaust
Intake
Exhaust
Sterilizer Sterilizer
Intake
"Dead" Air Space
Air flow washes entire room. Air movement is toward operator and
Air movement is away from operator. "dead" air spaces can form.
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Site Planning Worksheet

It may be helpful to use the provided Site Planning Worksheet (ANNEX B) to sketch the architectural
details of the location where the equipment will be installed. Include all details, such as walls,
doorways, structural supports, ventilation ducts (intake and exhaust), and electrical outlets (Figure 4).
Indicate any equipment that will be removed. The blank worksheet can be duplicated by the purchaser.
Figure 4. Site Planning Example

Equipment to be removed
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Proposed Location of Equipment

Using the completed sketch on the Site Planning Worksheet, complete an Equipment Location
CAUTION Worksheet (ANNEX B) to show the location and size of each piece of equipment in the work area
To reduce patient risks associated with (Figure 5). Include all other hard good items in the room (e.g. work tables, storage cabinets, etc.),
exposure to potentially non-sterile devices as this will help to assess the work flow.
or inadequate sterilization procedures, do not
install 3M™ Steri-Vac™ Sterilizer/Aerator GS Series After placing the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series and any accessory equipment on the
near any device emitting strong electronic magnetic Equipment Location Worksheet, indicate on the Worksheet any additional services required for the new
fields (EMFs). equipment. Provide the worksheets and service requirements to any contractors (electrical, ventilation,
plumbing, and structural) involved with the project.
Figure 5. Work Area and Equipment Location Example
51 cm Flammable
(20 in.) Abator
10 cm Indicator Exhaust Vent Liquid
CLR
(4 in.) Abator Panel Storage
CLR Cabinet
51 cm
(20 in.) GS8 Prep Table
CLR
(20 in.)
51 cm
SERVICE
CLR
Prep Table
Cart
ROOM
EO STERILIZER AND
GS5 OPERATOR ROOM
below
GS5 above
Prep Table
(20 in.)
51 cm
CLR
Abator
51 cm Abator 51 cm
Indicator
(20 in.) (20 in.)
CLR CLR Panel
10 cm
(4 in.)
CLR
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The 3M™ Steri-Vac™ Sterilizer/Aerator GS Series, Model GS5 can be installed in-wall or installed and
used with a 3M™ Stacking Rack Model 1237 as shown in Figure 6. The 3M™ Steri-Vac™ Sterilizer/
Aerator GS Series, Model GS8 is typically installed in-wall (Figure 7).
Figure 6. Typical In-wall Opening Requirements for 3M™ Steri-Vac™ Sterilizer/
Aerator GS Series, Model GS5
195.0 cm
(77 in.)
106.7 cm
(42 in.)
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Figure 7. Typical In-Wall Opening Requirements for 3M™ Steri-Vac™ Sterilizer/

Aerator GS Series, Model GS8
189.2 cm
114.3 cm (45 in.) (74.5 in.)
188.0 cm (74 in.) Max.
182.9 cm (72 in.) Min. Min. Depth
111.8 cm (44 in.) Max.

104.1 cm (41 in.) Min.
108.0 cm
(42.5 in.) 114.3 cm
(45 in.)
Pre-Installation Visit and Site Readiness Verification

Prior to the installation of the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series and any other accessory
equipment, the 3M Health Care service personnel or authorized 3M service personnel can be
contacted to visit the facility where the equipment will be installed. The proposed Site Planning and
Equipment Location Worksheets must be reviewed to discuss the required services, equipment
spacing, and any additional considerations. A Site Readiness Verification Form (ANNEX C) must be
completed and documented with the purchaser.
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IV. Preparing the Area and Service Requirements

Preparing the Selected Area
Once the location is selected and designed, the next step is to prepare the area. This section provides
details on the basic service connections required for the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series
and accessory equipment. Additional services may be needed for other equipment installed in order to
support the GS Series sterilizer equipment.
Note: The 3M™ Steri-Vac™ Sterilizer/Aerator The following equipment is needed to prepare the area:
GS Series will remain locked for three (3) hours
• An air compressor to supply clean, dry, oil-free • A ventilation system connection to local exhaust
for mandatory aeration without a connected and
air for the sterilizer vacuum system. hoods (as applicable).
operational local exhaust hood.
• If required by national, state, or local regulations • Ethernet connection for service and other
or facility/company policy, an ethylene oxide electronic interfaces.
(EO) emission control system.
Utilities
Consider the placement of utility services required for additional equipment. Obtain documentation
from supplier(s) for additional non-3M equipment and understand and implement all applicable
installation and service requirements for this equipment.
Table 3 provides detailed information for contractors installing the utilities and services that are required
to safely use the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series and accessory equipment. This Guide,
or individual pages from this Guide, can be photocopied and provided to contractors involved with the
project. The information, figures, and project worksheets are intended to provide examples of before
and after installation of the equipment in order to provide contractors with an understanding of the
project scope and requirements. Figure 8 shows typical service connections for the GS Series sterilizer.
Figure 8. Typical Service Connections for the GS Series Sterilizer, Model GS8
22.5 cm 23.0 cm
(57.15 in.) (58.42 in.)
26.0 cm
(66.04 in.)
31.75 cm
(80.65 in.)
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Electrical Service Requirements

The electrical service requirements for the installed 3M equipment are shown in Table 3. Be sure to
provide sufficient access to the power disconnect and switch. When planning the electrical service,
consider support equipment including: compressors, air dryers, and emission control systems.
Table 3 – Electrical Service Requirements

WARNING
To reduce the risk of shock due to Requirement GS5 Sterilizer/Aerator GS8 Sterilizer/Aerator
hazardous voltage, purchaser must provide
Voltage 200–240 Vac
a properly grounded outlet (an earth ground) for
installation, per applicable codes and regulations. Frequency 50/60 Hz
Phase Single
Current 15 amp dedicated circuit
WARNING Heat Load 5500 Btu/hr 6150 Btu/hr
Internal Circuit Breaker 7 amp 12 amp
To reduce the risks associated with fire
and explosion, purchaser must comply with Power Cord 240 volt, 15 amp, NEMA 6-15 plug2
applicable codes and regulations as they pertain Marks FCC cULus RCM CE0086 FCC cULus RCM CE
to locating the equipment and providing services
Due to variation in local regulations, the purchaser is responsible for complying
to the equipment. Code and Building
with applicable codes and regulations as they pertain to locating the equipment
Regulation Compliance
and providing services to the equipment.
Seismic Bracing kits for 3M™ Steri-Vac™ Sterilizer/Aerator GS Series, Models GS5
Seismic Bracing and GS8 units are available from 3M. For information on the State of California
pre-approved seismic bracing certificates, contact 3M.
UL listed to U.S. and Canadian Safety Standards

RCM Compliant with all applicable regulatory arrangements (RCM)
FCC (Federal Communication Commission)
Conformity to European Directives
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Compressed Air Requirements

Compressed air is used to operate a venturi vacuum generator and to operate the air-controlled pistons
that both lock and unlock the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series door. Table 4 provides
the compressed air requirements. The vacuum operates during the sterilization cycle to remove air
and ethylene oxide (EO) from the GS Series sterilizer chamber. The vacuum also operates during the
Aeration stage, which may last in excess of 12 hours.
DANGER Moisture in the compressed air line will not be removed by the supplied filter. A refrigerated air dryer
To reduce the risks associated with may be needed to meet the dew point requirement in Table 4 and should be a non-cycling hermetic
exposure to ethylene oxide, ensure type compatible with the flow and pressure of the selected compressor. The air dryer should be
compressed air supply is clean, with a maximum capable of accepting saturated air and drying it to 10°C (50°F) dew point at 38°C (100°F) ambient.
allowable dirt particle size of 0.5 microns, and The air dryer would typically have an automatic drain trap and be wired from the compressor controller.
oil-free. Ensure air filters on compressed air
supply contain a water trap and are cleaned
and maintained properly.
Table 4 – Compressed Air Specifications
Specifications Value/Range
7.0 kg/cm2 (100 psig) minimum
Pressure
10.5 kg/cm2 (150 psig) maximum
2.2 liters per second at 5.6 kg/cm2 (4.7 cubic feet per minute at 80 psig)
Flow Rate
per Sterilizer/Aerator based on 100% duty cycle compressor
Quality Clean air supply with a maximum allowable dirt particle size of 0.5 microns and free of oil
Moisture Content Less than 10°C (50°F) dew point
If the compressed air source does not meet the specifications, it can cause early equipment failures.
The GS Series sterilizer warranty and preventive maintenance agreements do not cover equipment
failures caused by an improper compressed air source. Contact the 3M Health Care Service Center or
your local 3M office for additional information regarding warranty and preventative maintenance plans.
The following refrigerated air dryer is an example of equipment that may be used:
Model: Arrow F-10
Supplier: Arrow Dryers
Website: www.arrowpneumaticdryers.com
Telephone (U.S.): 1-800-761-4298
Compressor System
The following recommended compressor manufacturer can provide additional information about
compatible compressor systems:
Supplier: Powerex Outside of the U.S., contact your local 3M Health Care
Website: www.powerexcompressors.com service personnel or authorized 3M service personnel
Telephone (U.S.): 1-800-761-4298 for local suppliers of equipment that meets the
required specification.
17 70-2011-5643-0 Issue Date: 10/2015

Filters
A 3M air line filter kit is needed and supplied with each 3M™ Steri-Vac™ Sterilizer/Aerator GS Series to
remove dirt and mist particles from the incoming air. This filter must be installed on the compressed
air line at the time of equipment installation and must be drained periodically by the purchaser in order
to remove excess water. These filters are replaced at each recommended six month preventative
maintenance service procedure.
The installation includes installing the 0.3 micron filter element (mist separator) in front of the
0.1 micron filter element (micro mist separator) in order to remove coarse air contaminants that would
otherwise plug the micro-mist element. The elements may need to be changed more frequently than
six month intervals if the air supply is highly contaminated.
The purchaser is solely responsible for providing a dry, oil-free air supply (to a dew point of 10°C/50°F).
Filters are provided for precautionary purposes only, and not as a replacement for a clean air supply.
A contaminated air supply can quickly reduce the effectiveness of the filter element, resulting in early
equipment failure.
Multiple Sterilizer/Aerator Installations

Each 3M Steri-Vac GS Series sterilizer requires a minimum flow rate of 2.2 liters per second
(4.7 scfm) at 5.6 kg/cm2 (80 psig) pressure. Two sterilizers would require a flow rate of
4.4 liters per second (9.4 scfm) air flow at 5.6 kg/cm2 (80 psig).
Compressed Air Line Installation Kit

The Compressed Air Line Installation Kit, supplied with each GS Series sterilizer, is installed between
the sterilizer and the compressed air services as shown in Figure 9. The purchaser is responsible for
providing compressed air services.
Compressor Location
The compressor should be located away from work areas in order to reduce noise levels around the
GS Series sterilizer. Make sure the compressor manufacturer’s electrical power requirements are met.
Figure 9. Compressed Air Line Connection Details
(Using Installation Kit)
Sterilizer
⁄ " NPT
14
2" Long
0–160
Nipple
PSI
Gauge 1⁄4" NPT
× 1⁄4" NPT
90° Elbow
7' High Pressure

Flow Flex Air Line
Shut Off Valve
⁄ " NPT × .625 Tube Adapter
14
14 ⁄ " Tee
⁄ " NPT
14
Union
⁄ " Hex Nipple
14
⁄ " NPT TO
14
⁄ " NPT Bushing

3 8
Optional
If required Micro Mist Separator
(Included ⁄ " Hex Nipple
14
in kit) Mist Separator
1⁄4" NPT, 90° Street Elbow
18 78-0803-3481-3 – Rev A. Issue Date: 8/2015

Ethylene Oxide Vent Line Requirements

A connection must be made from the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series to a dedicated vent
DANGER line in order to exhaust ethylene oxide (EO) to the outside atmosphere or to the 3M™ Abator emission
To reduce the risks associated with control system. The requirements for venting the GS Series sterilizer must be met (Table 5).
exposure to ethylene oxide:
a connection must be made from the Table 5. Vent Line Requirements for GS Series
3M™ Steri-Vac™ Sterilizer/Aerator GS Series to a Number of Sterilizer per Abator Length and Diameter of Vent Line
dedicated vent line to exhaust ethylene oxide (EO)
to the outside atmosphere or to the 3M™ Abator ≤ 31.0 m 31.1 m to ≤ 61.1 m to ≤
Length
emission control system. (100 ft.) 61.0 m (200 ft.) 91.5 m (300 ft.)
1
ensure the vent line is gas tight from the GS Series 2.54 cm
Diameter 2.54 cm (1 in.) 2.54 cm (1 in.)
sterilizer to the outside atmosphere. (1 in.)
≤ 31.0 m 31.1 m to ≤ 61.1 m to ≤
do not terminate vent line into exhaust system that Length
(100 ft.) 61.0 m (200 ft.) 91.5 m (300 ft.)
recirculates air into the building. 2
Diameter 2.54 cm (1 in.) 3.8 cm (1.5 in.) 3.8 cm (1.5 in.)
the vent line should terminate away from areas
where people walk or work. The vent line should The 3M EO Abator can be used with the GS Series sterilizer with a maximum of two GS Series
be located at least 7.6 m (25 ft) away from the
building air intake source. sterilizers and up to a maximum of two 3M Aerator models XL or XLS connected to a single EO Abator
unit. Sterilizer models 5XL and 8XL cannot be combined with a GS Series sterilizer when connecting to
vent line must be labeled to indicate EO. an EO Abator. The EO Abator interfaces with GS Series sterilizers to start and stop automatically.
ensure no blockages in vent line exist.
The diameter of the vent line used for the EO inlet and safety vent depends on the combined length of
ensure the instructions detailed in this Guide are the two vent lines. The size of the copper tubing to connect sterilizer discharge to the EO Abator system
followed when planning and installing the ethylene EO inlet should be between 2.5 cm (1.0 in) and 3.8 cm (1.5 in). The size of the National Pipe Thread
oxide vent line.
(NPT) connection at the EO Abator system should be 1.9 cm (3/4 in.). Reference Table 5 for required
line diameters.
The maximum length of the vent line from the GS Series sterilizer port is 91.5 meters (300 feet).
Do not exceed this specification. The use of Type K hard drawn copper tubing is recommended.
The vent system should be constructed of straight lengths of copper tubing using a minimum number
of long radius elbows. Short radius elbows and T fittings cause an excessive amount of back pressure
and should not be used. Include a threaded fitting to termination of the run with which to facilitate the
pressure test of the system.
The vent line should be designed to avoid sags or loops in order to prevent moisture buildup at other
points within the vent line. The vent line must be gas tight from the sterilizer to the outside atmosphere
and be brazed or soldered in accordance with local fire codes.
The vent line, with the exception of a turned-down extension terminating on the roof top or exterior wall,
should be inside the building in order to prevent moisture from freezing in the vent line and blocking the
vent (Figures 10, 11 and 12).
3M Abator (Emission Control Devices)

3M Abators (Models 50AN, 50AE or 50AJ) can be connected to and are compatible with the
3M Steri-Vac Sterilizer/Aerator GS Series. Consult the 3M Abator Operation and Installation Manual
for further information.
19 70-2011-5643-0 Issue Date: 10/2015

Vent Line Labeling and Install Considerations

The vent line contains significant amounts of EO during the Gas Removal and Flushing stages. Ensure
the vent line is gas tight from the GS Series sterilizer to the outside atmosphere and is labeled to
indicate EO. A separate vent line to the outside is required. The vent line should terminate away from
areas where people walk or work and should be located at least 7.6 m (25 ft) away from the building
air intake source.1
Do not terminate the vent line within 7.6 m (25 ft) of any possible source of ignition or any opening to
the building interior such as fresh air inlets, unsealed windows, or pedestrian traffic areas. The inlet
assembly, from the Vent Line Installation Kit, must be installed within 91.44 cm (3 ft) of the
sterilizer's EO port in a position that is accessible to 3M Health Care service personnel (Figure 10).
The single vent line is run directly to the exterior or to the 3M Abator using the appropriate connection
fittings. When the 3M Abator is installed, run the vent line from the vent outlet port on the 3M Abator
to the outside. Shut off valves in the vent line are not recommended.
1. AAMI/ANSI ST41 (2009) Ethylene oxide in health care facilities: Safety and effectiveness
Figure 10. Ethylene Oxide Vent Line Connection Details

(Using an Installation Kit)
⁄ " NPT, 2" Long Nipple

3 8
3 ⁄4" SWT to 1" Copper Line
⁄ " NPT to 3⁄4" SWT

3 8
7' Flexible Vent Line
⁄ " NPT Union

3 8
⁄ " NPT Elbow

3 8
Figure 11. Ethylene Oxide Horizontal Vent Line Installation Example
External Wall
Copper Line
Curved down
Steri-Vac minimize
Sterilizer/Aerator external
vent line
20 70-2011-5643-0 Issue Date: 10/2015

Figure 12. Ethylene Oxide Vertical Vent Line Installation Example
Minimum radius; two times

the tubing diameter
Roof
Insulation
Copper Line
(Maximum Length = Cupola
91.5 m/300 ft)
30.5 cm
5 cm 5 cm (12 in.)
(2 in.) (2 in.)
Steri-Vac
Sterilizer/Aerator
13 cm
(5 in.)
18 ga galvanized pipe
21 70-2011-5643-0 Issue Date: 10/2015

Local Exhaust Hood Requirements

The 3M™ Steri-Vac™ Exhaust Hood is an over-the-door exhaust (e.g. vent) hood that supplements the
room’s directional air flow, and is designed to draw air away from the Operator removing the load from
the chamber. The exhaust hood is connected by 3M Health Care service personnel or authorized 3M
service personnel to a purchaser-supplied dedicated exhaust system during installation.
Monitor the exhaust hood for appropriate air flow (Figure 13). If the 3M™ Steri-Vac™ Sterilizer/Aerator
GS Series detects the air flow is too low (<125 CFM) through the exhaust hood (or either of the exhaust
hoods if using a double door unit), the GS Series sterilizer door will remain locked until a minimum three
hours of aeration is complete. See the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series Operator Manual for
additional set-up information.
Figure 13. Air Flow to the Exhaust Hood
Exhaust Ventilation System Planning and Design

The following requirements must be met for planning and designing the ventilation system:
• Determine the required air flow and the size, length and number of elbows needed for the ductwork.
Take into consideration that each elbow introduces losses in air flow.
• Calculate the total air flow required for each branch.
• Calculate the static pressure for the entire system using standard industrial ventilation techniques, and
add a 10% safety factor to the air flow and the static pressure to determine the final air flow target.
• Select an exhaust fan to meet the defined requirements.
• Determine if a new exhaust system is needed or if an existing system can be used. If using an existing
system, make sure the existing system meets the GS Series sterilizer equipment specifications.
The diagrams in Figures 14 and 15 show installation options for consideration in planning for the
installation.
• Design and construct the exhaust system in accordance with national, state and/or local fire, health,
and safety codes.
Connect the hood to a dedicated exhaust system. The hood should not be connected to an exhaust
system that re-circulates air into the building.
22 70-2011-5643-0 Issue Date: 10/2015

Exhaust Ventilation System Specifications

The following ventilation system requirements must be met to ensure maximum air movement through
the hood.
Air flow Single Door Unit: Minimum of 3.5 cubic m/min (125 scfm) to the exhaust
hood connection, or a minimum of 350 m/min (1435 ft/min) in the
102 mm (4 in) line to the exhaust hood connection. Maximum air flow
through the hood is 7.0 cubic m/min (250 scfm).
Double Door Unit: Minimum of 7.0 cubic m/min (250 scfm to the exhaust hood
connection, or a minimum of 700 m/min (2870 ft/min) in the 102 mm (4 in)
line to the exhaust hood connection. Maximum air flow to the exhaust hood
connection is 14.0 cubic m/min (500 scfm).
Hood connection 102 mm (4 in) outside diameter
Ductwork
• Use metallic ductwork rated to handle the highest pressure that the system delivers. Use a minimal
amount of flexible, air-tight duct. A flexible duct can introduce significant air flow resistance.
• Use a larger diameter flexible duct to minimize frictional air drag loss.
• Minimize the number of elbows to reduce the static pressure loss in the system.
• Seal duct seams and joints with aluminum duct tape or sealant to prevent leaks. The duct does not
have to be gas tight.
• Ensure the ductwork material is impervious to ethylene oxide(EO).
Exhaust Fan
• Use a centrifugal fan with backward curved blades designed for continuous operation.
• Use a high efficiency spark-proof fan with the motor sealed from the exhaust air stream.
• Use an impeller and impeller ring around the drive shaft that is nonferrous.
Ventilation Failure Detector

An air flow sensor is installed in the exhaust opening of the hood as standard equipment. The sensor
detects low air flow in the exhaust hood and activates a Caution message (E501 - Exhaust Hood
Air Flow) to alert personnel of ventilation system failure. This Caution message does not stop the
sterilization cycle in progress, but will cause the performance of an automatic three-hour locked,
mandatory aeration. The ventilation problem must be corrected in order to clear the Caution message.
23 70-2011-5643-0 Issue Date: 10/2015

Figure 14. Exhaust Connection
Exhaust Hood Duct
Alternate Connection for

Exhaust Hood Duct
Figure 15. Multiple Exhaust Hoods Vented into a Dedicated Ventilation System
24 70-2011-5643-0 Issue Date: 10/2015

First Aid: Exposure to Ethylene Oxide (EO)
Inhalation:
DANGER Move the person to fresh air and seek medical attention.
To reduce the risks associated with Skin or Clothing Contact:
exposure to ethylene oxide:
Immediately wash with soap and water. Remove contaminated clothing and wash before reuse.
Only use 3M™ Steri-Gas™ 100% Ethylene Oxide
If signs/symptoms develop, seek medical attention.
(EO) Gas Cartridges as listed in this Guide. Do not
use other brands or types of sterilant cartridges. Eye Contact:
Do not use damaged 3M Steri-Gas EO Gas
™ ™
Immediately flush with large amounts of water for at least 15 minutes. Remove contact lenses
Cartridges. if easy to do so. Continue rinsing. Immediately seek medical attention.
If Swallowed:
Rinse mouth. DO NOT INDUCE VOMITING. Immediately seek medical attention.
Hazard Statements of Ethylene Oxide (EO):
• Extremely flammable gas • May cause drowsiness or dizziness
• Contains gas under pressure, • Suspected of damaging fertility
may explode if heated or an unborn child
• Toxic if inhaled • May cause cancer
• Causes serious eye irritation • May cause genetic defects
Ethylene Oxide Storage

For additional information, go to www.3M.com to obtain the 3M™ Steri-Gas™ EO Gas Cartridge Safety
Data Sheet (SDS). Follow specific storage requirements for storing Steri-Gas EO Gas Cartridges.
WARNING Check national, state and local regulatory requirements, including fire protection codes, for storing EO.
To reduce the risks associated with fire Store Steri-Gas EO Gas Cartridges in an approved flammable liquid storage cabinet that vents to
and explosion: the outside, through a non-recirculating, continuously operating, dedicated exhaust system, or in an
3M™ Steri-Gas™ EO Gas Cartridges contain area suitable for storage of flammable liquids that appropriately vents to the outside. Keep all sources
100% Ethylene Oxide (EO), which is an extremely of ignition (e.g. matches, lit cigarettes, sparks and static discharge) away from the 3M™ Steri-Vac™
flammable gas and liquid under pressure. Do not Sterilizer/Aerator GS Series and 3M™ Steri-Gas™ EO Gas Cartridges.
use near flame, electrical spark, hot surfaces, or One (1) box of twelve (12) Steri-Gas EO Gas Cartridges can be stored at least two meters (6.5 ft)
allow sources of ignition near the cartridges. from the Operator desk or work station that is designed and verified with 10 air exchanges per hour.
Do not puncture cartridge outside the sterilization Amounts greater than one box of Steri-Gas EO Gas Cartridges must be stored in a flammable liquid
chamber. Do not incinerate cartridges. Exposure storage cabinet as described. Follow all national, state and local regulations for ethylene oxide storage.
to temperatures above 150ºF (65.5ºC) may cause
cartridge to burst.
Do not attempt to access any internal mechanisms
of the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series.
Operators should not service the sterilizer as there
are no user serviceable parts.
25 70-2011-5643-0 Issue Date: 10/2015

Requirements for a Vented Cabinet

The following are requirements for ethylene oxide (EO) gas cartridge storage:
• Flammable storage cabinet has venting capability. Size of cabinet is based on the amount of planned
and stored EO – typically one to two months supply.
• SECURALL® cabinets are one type of cabinet that can be used for storing EO. These types of cabinets
can be purchased through Grainger, a vendor with international access. Product information is
available at: www.grainger.com.
• Use metal tubing, which can be flexible tubing with stainless steel foil for use outside of a wall;
or, use rigid metal tubing for use within a wall.
• A centrifugal fan, with backward curved blades designed for continuous operation, is required to
exhaust the cabinet in a dedicated exhaust system. The fan must be a high efficiency spark-proof
fan with the motor sealed from the exhaust air stream. The impeller and impeller ring around the
drive shaft must be nonferrous. The fan size is based on cabinet size, length of run, and air flow
requirements. The fan size should be determined by the facility’s heating, ventilation, and air
conditioning experts and should be capable of providing 10 air exchanges per hour inside the cabinet.
Connect EO Storage Cabinet to GS Series Sterilizer Dedicated Exhaust

The vent for the storage cabinet can be connected into the overhead exhaust that is dedicated to the
3M™ Steri-Vac™ Sterilizer/Aerator GS Series exhaust as a non-recirculating system. With this
configuration, no additional fan is needed. Connecting the cabinet to the system should follow these
steps (Figure 16):
• Remove both metal bungs from the sides of the cabinet and replace flame arrestor screens (normally
these come with the cabinets) into the openings.
• Connect the bottom opening to the GS Series sterilizer exhaust vent (or separate exhaust fan) using
metal tubing. Tubing must have an inner diameter no less than that of the opening.
• The piping should be sealed and is not required to be gas tight. Weld the seams for rigid metal tubing.
For flexible tubing, seal with aluminum duct tape or sealant. The length of tubing should be verified in
order to allow a minimum of 10 air exchanges per hour in the cabinet.
• The top opening shall serve as the fresh air inlet. The make-up air should be supplied to the fresh air
inlet in tubing similar to that used for the exhaust.
• The discharge point for the outside exhaust should be at least 7.6 m (25 ft) away from any possible
sources of ignition, openings to buildings, or pedestrian traffic ways.
Figure 16. Vented EO Storage Cabinet Connection to Dedicated Exhaust
Tie to 3M™ Steri-Vac™ Intake

Overhead Exhaust Vent Air
Flame
Arrestor
Flame
Arrestor
26 70-2011-5643-0 Issue Date: 10/2015

Disposal of 3M™ Steri-Gas™ EO Gas Cartridges

Empty 3M™ Steri-Gas™ EO Gas Cartridges should be aerated for a minimum of two (2) hours before
disposal. The empty cartridge can aerate while located inside the GS Series sterilizer chamber
cartridge holder during a normal aeration cycle. After aeration is complete, remove the cartridge
from the holder and dispose of it in non-incinerated waste or recycle per your facility’s requirement.
See ANNEX E for additional information related to the proper handling of ethylene oxide (EO).
Outside Discharge
The ventilation system should exhaust to the outside. Use a roof-top discharge. The discharge point
should be at least 7.6 m (25 ft) away from any possible sources of ignition, openings to building, or
pedestrian traffic ways. Greater distances may be needed in some locations. Use one of the types
of discharge terminations illustrated in Figure 17.
It may be helpful to work with an industrial ventilation consultant or ventilation contractor to help
design and install the local exhaust system.
Figure 17. Recommended Outside Ventilation Stack Design
Stack
Drain Plug
Updraft Discharge Elevated Tube with 15° Taper No Loss Stack
27 70-2011-5643-0 Issue Date: 10/2015

V. Final Installation and Support

Only qualified service personnel should install and service this equipment. Do not plug the cord into an
outlet or operate the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series until 3M Health Care service personnel
WARNING or authorized 3M service personnel have completed final installation support activities, including an
To reduce the risks associated with fire and in-service training and the safe handling of ethylene oxide (EO) training for Operators.
explosion, do not attempt to access any internal
mechanisms of the 3M™ Steri-Vac™ Sterilizer/ Site Readiness Verification
Aerator GS Series. Operators should not service
the sterilizer as there are no user serviceable parts. A Site Readiness Verification must be conducted by 3M Health Care service personnel or authorized
3M service personnel with the purchasing facility.
The purchaser of the GS Series sterilizer and any accessory equipment should complete the Site
WARNING Readiness Verification Form (ANNEX C) and provide the form to the designated 3M Health Care service
To reduce the risk of shock due to personnel or authorized 3M service personnel to review prior to the scheduled installation date. During
hazardous voltage: this review, the 3M service personnel will discuss any changes required before final installation support
Do not attempt to access any internal mechanisms and verification can be completed by 3M.
of the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series.
Operators should not service the sterilizer as there Unpacking the GS Series Sterilizer
are no user serviceable parts.
The purchaser will unpack and inspect the GS Series sterilizer as follows:
Use only trained 3M Health Care or authorized
3M service personnel for installation support 1. Remove all shipping material from the sterilizer.
and maintenance. 2. Examine the sterilizer for damage. If any shipping damage is found when unpacking the sterilizer,
Do not modify any part of 3M Steri-Vac Sterilizer/ immediately file a damage claim with the transportation company and notify your 3M sales or
Aerator GS Series. service representative. Typically, a transportation company assumes liability for shipping damage
for a 10-day period starting with the day of delivery. After the 10 days, the purchaser must accept
Use only 3M designated replacement parts. the merchandise as delivered.
3. Discard packaging per 3M recommendations; reference ANNEX F for details.
DANGER 4. Position the sterilizer in its permanent location and level the unit by adjusting the sterilizer feet.
The position of the sterilizer must allow a minimum of 51 cm (20 in) on each side and on top
exposure to ethylene oxide (EO):
of the unit for service access.
Vent line must be labeled to indicate EO.

Once the GS Series sterilizer is in place and is connected to the required electrical and mechanical
services, it is ready for final installation support by 3M Health Care service personnel or authorized
3M Health Care service personnel or authorized 3M service personnel.
3M service personnel must verify that final
installation checks are completed.
28 70-2011-5643-0 Issue Date: 10/2015

System Checkout and In-Service Training

3M Health Care service personnel or authorized 3M service personnel will provide installation support
and assure that the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series is installed and operating according to
3M specifications. At final installation, the 3M Health Care service personnel or authorized 3M service
DANGER
personnel will:
exposure to ethylene oxide: • complete the final Installation Verification Form and request signature by the purchaser’s
authorized personnel.
It is the user’s facility management’s responsibility
to ensure that all personnel working with • provide a completed Customer Service Order that includes the date the warranty takes effect.
toxic chemicals, gases, and vapors are given • provide in-service training for purchaser facility personnel on the proper operation of the
comprehensive instruction in the process. This GS Series sterilizer and any accessory equipment.
instruction includes information on relevant health
hazards; national, state and local regulations • provide in-service training on the safe handling of ethylene oxide (EO) and information on a
methods for safe use; and methods to detect 3M™ Steri-Vac™ Gas EO Sterilization Operator Certification Program.
escape of the agent. • review ANNEX A for first aid information related to EO exposure.
It is the user’s facility management’s responsibility
to ensure regular training of all personnel
concerned with the operation and maintenance of
the equipment, including emergency procedures
for any toxic, flammable, or explosive material
released into the environment. Records of
attendance at training are maintained, and
evidence of understanding demonstrated.
29 70-2011-5643-0 Issue Date: 10/2015

VI: Install Guide for 3M™ In-Wall Mounting Unit

General Information
The 3M™ In-Wall Mounting Unit 1238 is a kit that contains the 3M™ Stacking Rack 1237 along with a
Note: All figures for this section stainless wall bezel and front trim for flush mount installation as shown in Figure 18. The Stacking Rack
are located at the end of is a two level apparatus that holds two 3M™ Steri-Vac™ Sterilizer/Aerator GS Series, Model GS5 or one
Section VI for reference. GS Series sterilizer, Model GS5 and one 3M™ XL Aerator.
The purchaser should understand and comply with all national, state and local regulations related to
installing the In-Wall Mounting Unit 1238.
To begin the installation process, remove the Stacking Rack 1237 from its shipping carton.
Be sure to check for any shipping damage and report any damage immediately to the shipping
company. Inspect the major components as depicted in Figure 20.
To prepare the In-Wall Mounting Unit 1238 for installation, remove the feet from the bottom of the
Stacking Rack 1237 and install the supplied casters using 5/16 × 1 inch bolts, nuts and washers.
Turn the Stacking Rack over so it is sitting on the casters and locate the upper frame and joining tabs.
Attach the joining tabs to the upper frame with 5/16 × 1 inch bolts. Remove two of the plastic caps from
the front of the Stacking Rack and install the upper frame as shown in Figure 19.
General Specifications
The Access Area is the space into which the In-Wall Mounting Unit 1238 is placed. The access area
must be well ventilated:
• to maintain an ambient temperature of not greater than 35°C (100°F). Higher ambient
temperatures may impact the Sterilizer/Aerator 38°C cycle temperature or cause 38°C cycle
to abort.
• by having a minimum of 10 air exchanges per hour.
Finished Installation
• Figure 18 provides a diagram of a completed installation. This example shows a GS Series sterilizer,
Model GS5 on the top shelf and a second GS Series sterilizer, Model GS5 on the bottom shelf.
• Figure 21 shows the dimensions of the door frame opening required for the In-Wall Mounting Unit.
• Figure 22 shows the wall preparation for a double door GS Series sterilizer pass-through
configuration.
30 70-2011-5643-0 Issue Date: 10/2015

Finished Wall Specifications

A finished wall opening should meet the following dimensions:
Height: 195.58 cm +1.27/- 0 cm (77 in. + 1/2 /-0 in.)
Width: 106.68 cm +1.27/- 0 cm (42 in. + 1/2 /-0 in.)
Depth: Minimum of 106.68 cm (42 in.)
The finished walls must be plumb. If a side wall is in front of the 3M™ Steri-Vac™ Sterilizer/Aerator
GS Series, there must be a distance of 50.8 cm (20 in.) between such a wall and the 3M™ In-Wall
Mounting Unit 1238 to allow for service access when the unit is rolled out of the access area.
Floor Preparation
The floor finish in the area housing the unit must be the same height (i.e. on the same plane) as the
work area in front of the unit for ease of movement for unit service and repair. The floor finish area
should be flat and level with dimensions of:
Width: 106.68 cm minimum (42 in.)
Depth: 106.68 cm minimum (42 in.)
The GS Series sterilizer must be available for fitting onto the unit at the time of installation since some
adjustments may be necessary when attaching the front panels.
Installing Permanent Floor Channels

Reference Figure 23.
Use of the template:
• A blueprint marked “TEMPLATE, Model 1238” is included with the 3M™ In-Wall Mounting Unit
Model 1238.
• Lay the TEMPLATE in the access area with the front aligned with the front wall of the DOOR FRAME.
• If the TEMPLATE does not fit properly, check the DOOR FRAME width for uniformity, top-to bottom,
and shim as needed.
• Tape the TEMPLATE down, being careful to obtain as much surface contact of the TEMPLATE to the
floor as possible.
• Mark and drill at least four (4) holes per the FLOOR CHANNEL.
• Remove the TEMPLATE.
• Anchor the FLOOR CHANNELS to the floor using suitable concrete anchors. Do not over tighten the
bolts at this time, as it may be necessary to adjust the FLOOR CHANNELS later in the installation.
• Attach the STOP BRACKET as illustrated in Figure 24. Temporarily adjust the STOP BRACKET to its
farthest rear position. It will be readjusted later in the installation.
31 70-2011-5643-0 Issue Date: 10/2015

Placement of 3M™ Steri-Vac™ Sterilizer/Aerators onto the Stacking Rack

• Roll the STACKING RACK onto the permanently mounted FLOOR CHANNELS.
• Attach the EXTENSION TRACKS to the FLOOR CHANNELS.
• Roll the STACKING RACK forward onto the EXTENSION channels as illustrated in Figure 26.
• Position the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series onto the top tray of the STACKING RACK.
Position the front of the GS Series sterilizer as illustrated in Figure 27. CAUTION: Due to the weight of
the Sterilizer/Aerator, this procedure will normally require at least three (3) individuals.
• Secure the GS Series sterilizer to the top tray by means of the provided 5/16 × 1 1/2 in. bolts, washers,
and nuts.
• Follow the same procedure for mounting the Aerator to the bottom tray of the STACKING RACK.
Observe the same precautions.
• Adjustments: The front plane of both GS Series sterilizers must be approximately parallel with the
front plane of the STACKING RACK. If adjustments are needed, use the ADJUSTABLE NYLON FEET
for this purpose.
Access Area
Figure 28 is a generalized drawing of the service connections at the rear of the installation. As
previously described, flexible lines are required between the GS Series sterilizer and the stationary
services. The connections need not be made until installation is complete.
Installation of Stainless Steel Panels

• Remove the protective adhesive-backed paper from the PANELS prior to installation. During
installation, use care so as to not scratch the stainless steel surfaces.
• Beginning with the TOP PANEL, attach the top and lower PANELS to the STACKING RACK by means
of the Phillips-head STAINLESS SCREWS. Leave all of the screws loose at this time.
• Do not attempt to install the LOUVERED PANEL at this time.
• Slide the left and right doors frames in behind the STAINLESS STEEL PANELS and tighten the
screws.
• Slide the top door frame in behind the top STAINLESS STEEL panel. Align the door frames and
tighten all of the panel screws. Install the nut and washer on either end of the top door frame.
• Locate the adhesive backed foam and place it around the back side of the door frame at the outer
edge (Figure 25).
• Gently roll the STACKING RACK back into the access area until the DOOR FRAME meets the wall.
32 70-2011-5643-0 Issue Date: 10/2015

Stop and Hook Adjustment

• The purpose of the STOP is to keep the STACKING RACK/STAINLESS STEEL PANELS from
damaging the flange on the DOOR FRAME when returning the unit to the access area after service
and maintenance.
• Remove the STOP from the right FLOOR CHANNEL. Apply a liberal coating of petroleum jelly to both
the bottom of the STOP and the floor area beneath the STOP.
• Reattach the STOP loosely to the FLOOR CHANNEL, this time in its forward-most position.
• Gently roll the unit back into the access area until contact is barely made between the STAINLESS
STEEL PANELS and the flange on the DOOR FRAME.
• Carefully roll the unit forward, again, and tighten the STOP. Be careful not to move the unit forward
or rearward during this process.
• The purpose of the HOOK is to keep the unit from rolling forward as operators open and close
Sterilizer/Aerator doors.
• Attach the HOOK on the bracket on the lower left comer of the STACKING RACK. Attach the shoulder
bolt and three washers on the outside of the left FLOOR CHANNEL (Figure 20).
• With the unit tight against the STOP, adjust the HOOK so that firm contact is made between the
HOOK and SHOULDER BOLT (Figure 24).
• Tighten the nut on the shaft of the HOOK to maintain the HOOK position.
Flexible Connections
• Connect all electro-mechanical services to the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series
(e.g. compressed air, vent line, exhaust hood and electrical).
• Observe all flexible connections while rolling the unit back into the access area. Make sure
that none of these lines fall down into the FLOOR CHANNELS where they might become damaged
by the wheels on the STACKING RACK.
Installing the Louvered Panel

• Roll the unit back into the access area and secure the HOOK.
• Remove the EXTENSION TRACKS and store them beneath the unit.
• Attach the LOUVERED PANEL.
• Installation is now complete.
33 70-2011-5643-0 Issue Date: 10/2015

Figure References for Section VI
Figure 18. Installation Print No. 1: In-Wall Mounting Unit 1238 Showing
Stacking Rack
Figure 19. 3M™ In-Wall Mounting Unit 1238 Components
34 70-2011-5643-0 Issue Date: 10/2015

Figure 20. Installation Print No. 2: 3M™ In-Wall Mounting Unit Model 1238
Illustrated Parts List
⁄ " Stainless
14
Screws
24 ea.
Top Panel
1 ea.
Top Channel
1 ea.
Lower Upper Frame

Panel Stop
1 ea. Permanent 1 ea.
1 ea. Floor Channel
2 ea.
Joining
Tabs
Louvered 2 ea. Fastener
Panel ⁄ " × 20" Stud
14
1 ea. Hook
Assembly ⁄ " Washer
14 12 ea.
⁄ " × 1"
5 16 1 ea. 8 ea.
⁄ " × 1"
14 Side Channel
Bolts L&R
16 ea. Bolt 2 ea.
8 ea.
Foam
Locking 40 3⁄8" 2 ea.
Bracket
1 ea.
10 7⁄8"
Casters
4 ea. ⁄ " Washer
5 16
⁄ " Nut
5 16 16 ea.
16 ea. Extension
Track
2 ea.
35 70-2011-5643-0 Issue Date: 10/2015

Figure 21. Installation Print No. 3: Figure 22. Installation Print No. 11: Model 1238 Pass Through
3M™ In-Wall Mounting Unit Model 1238 3M™ Steri-Vac™ Sterilizer/Aerator GS Series, Model GS5 Installation
Door Frame Opening
Processed Goods Side
195.6 cm
(77 in.)
34 1⁄ 8"
Distance
Between
Walls
106.7 cm 9" 42"

(42 in.) Min. Distance
for Multi-Unit Unprocessed Goods Side
Installations
Figure 23. Installation Print No. 5: Model 1238 Fastening Permanent

Floor Channels (Track)
Template
Supplied by
3M
Anchor
36 70-2011-5643-0 Issue Date: 10/2015

Stop and Hook Adjustment
Stop Shoulder Hook

Bolt
Figure 25. Installation Print No. 4: Model 1238 Mounting Door Frame In-Wall
37 70-2011-5643-0 Issue Date: 10/2015

Mounting Extension Tracks and Cart
38 70-2011-5643-0 Issue Date: 10/2015

Mounting Units to Cart
39 70-2011-5643-0 Issue Date: 10/2015

Figure 28. Installation Print No. 8: 3M™ In-Wall Mounting Unit Model 1238 Unit Rear Hookups
Note: Figure 28 shows a 3M™ Steri-Vac™ 200-240 Volt 200-240 Vent Line
Sterilizer/Aerator GS Series, Model GS5 on Supply for Volt for
Sterilizer as Supply for Sterilizer
the top shelf and a 3M™ Steri-Vac™ XL Aerator required Aerator
on the bottom. Service hookups will vary
based on configurations. Refer to the
3M™ Steri-Vac™ Sterilizer/Aerator GS Series Vent opening for
and 3M™ Steri-Vac™ XL Aerator Installation local exhaust
installation
Guides for specific requirements. (hospital-supplied
exhaust system
required)
Damper
Vent Duct
for Aerator
Boost
Transformer
(If Needed)
Compressed
Air Line
40 70-2011-5643-0 Issue Date: 10/2015

Figure 29. Installation Print No. 9: Mounting Top Two (2) Panels
Top Panel
Bottom Panel
41 70-2011-5643-0 Issue Date: 10/2015

Remove Extensions Mount Bottom Panel
42 70-2011-5643-0 Issue Date: 10/2015

Notes
43 70-2011-5643-0 Issue Date: 10/2015

ANNEX A Symbols, Safety Warnings and Cautions

Document Conventions 3M™ Steri-Gas™ EO Gas Cartridges – Explanation of
Explanation of Single Word Consequences
Label and Symbols
Danger: Indicates a hazardous situation which, if not avoided, will

Flammable Gas: Category 1
result in death or serious injury.
Warning: Indicates a hazardous situation, which, if not avoided, could

Caution: Indicates a hazardous situation, which, if not avoided, could Gas Under Pressure: Liquefied Gas
result in minor or moderate injury.
NOTICE: Indicates a hazardous situation which, if not avoided, may

result in property damage.
Acute Toxicity (inhalation): Category 3
3M Steri-Vac Sterilizer/Aerator GS Series –
™ ™
Explanation of Product and Packaging Label

and Symbols Specific Target Organ Toxicity (single exposure): Category 1
Attention: Refer to the Operator Manual for additional information. Specific Target Organ Toxicity (repeated exposure): Category 1
Specific Target Organ Toxicity (central nervous system): Category 3
Warning: Indicates a hazardous situation, which, if not avoided, could Carcinogenicity: Category 1A
Reproductive Toxicity: Category 2
Waste Electrical and Electronic Equipment (WEEE) and EU Battery
Germ Cell Mutagenicity: Category 1B
Directive. This symbol indicates that both the device and lithium ion
battery contained therein need to be disposed of properly. Eye Irritation: Category 2A
Skin Irritation: Category 2
UL Listed to U.S. and Canadian Safety Standards.
Danger
Mark of Conformity to European Directives.
Compliant to all applicable ACMA regulatory arrangements (RCM). DANGER: Potential health effects of ethylene oxide
Serial number: This symbol is accompanied by the serial number Users must follow the requirements of the United States Occupational
relevant to the device bearing the symbol. Exposure Standard for Ethylene Oxide OSHA (29 CFR 1910.1047).
100% ethylene oxide (EO) CAS number 75-21-8 is a colorless gas at
Catalog: This symbol is accompanied by the catalog number relevant ambient conditions. Do not rely on sense of smell for the detection
to the device bearing the symbol.
of ethylene oxide. Ethylene oxide has a high odor threshold and can
Authorized representative for the European Community: This symbol only be detected by sense of smell when it exceeds 500 – 700 parts per
is accompanied by the name and the address of the authorized million (PPM). Ethylene oxide has a characteristic ether-like odor,
representative in the European Community. a sweet and irritating solvent smell.
Manufacturer: This symbol is accompanied by the name and address
of the manufacturer.
Date of Manufacture: This symbol is accompanied by the date of

manufacture.
44 70-2011-5643-0 Issue Date: 10/2015

First Aid Warnings

Inhalation:
WARNING: To reduce the risks associated with fire and
Move the person to fresh air and seek medical attention. explosion:
Skin or Clothing Contact: 3M™ Steri-Gas™ EO Gas Cartridges contain 100% Ethylene Oxide (EO), which
Immediately wash with soap and water. Remove contaminated clothing and is an extremely flammable gas and liquid under pressure. Do not use near
wash before reuse. If signs/symptoms develop, seek medical attention. flame, electrical sparks, or hot surfaces, or allow sources of ignition near the
cartridge. Do not puncture the cartridge outside of the sterilization chamber. Do
Eye Contact: not incinerate cartridges. Exposure to temperatures above 65.5ºC (150ºF) may
cause cartridge to burst.
Immediately flush with large amounts of water for at least 15 minutes.
Remove contact lenses if easy to do so. Continue rinsing. Immediately seek Do not attempt to access any internal mechanisms of the 3M™ Steri-Vac™
Sterilizer/Aerator GS Series. Operators should not service the sterilizer as there
medical attention. are no user serviceable parts.
If Swallowed:
Rinse mouth. DO NOT INDUCE VOMITING. Immediately seek medical WARNING: To reduce the risk of shock due to hazardous
attention. voltage:
Do not attempt to access any internal mechanisms of the 3M™ Steri-Vac™
Hazard Statements of Ethylene Oxide (EO): Sterilizer/Aerator GS Series. Operators should not service the sterilizer as there
• Extremely flammable gas are no user serviceable parts.
• Contains gas under pressure, may explode if heated The purchaser must provide a properly grounded outlet (an earth ground), for
installation, per applicable codes and regulations.
• Toxic if inhaled
Do not operate the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series outside the
• Causes serious eye irritation environmental conditions as stated in this manual.
• May cause drowsiness or dizziness
Use only trained 3M Health Care service personnel or authorized 3M service
• Suspected of damaging fertility or an unborn child personnel for installation support and maintenance.
• May cause cancer
Do not modify any part of 3M™ Steri-Vac™ Sterilizer/Aerator GS Series.
• May cause genetic defects
Use only 3M designated replacement parts.
Reference – consult the 3M™ Steri-Gas™ EO Gas Cartridges Safety
Data Sheet (SDS) for additional information (www.3M.com).
Cautions
Dangers
CAUTION: To reduce the risk of injury,
DANGER: To reduce the risks associated with exposure
to ethylene oxide: always follow the procedures described in this 3M Site Planning and
Installation Guide.
Ensure a minimum of ten (10) air exchanges per hour (ACHs) for the room in
which the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series is installed.
Do not operate the 3M™ Steri-Vac™ Sterilizer/Aerator GS Series outside the
CAUTION: To reduce patient risks associated with exposure
environmental conditions as stated in this manual.
to potentially non-sterile devices or inadequate sterilization
Only use 3M™ Steri-Gas™ 100% Ethylene Oxide (EO) Gas Cartridges as listed in procedures,
this manual. Do not use other brands or types of sterilant cartridges.
Do not use damaged 3M™ Steri-Gas™ EO Gas Cartridges. do not install 3M™ Steri-Vac™ Sterilizer/Aerators GS Series near any device
Ensure compressed air supply is clean, with a maximum allowable dirt particle emitting strong electronic magnetic fields (EMFs).
size of 0.5 microns, and free of oil. Ensure air filters on compressed air supply
contain a water trap and are cleaned and maintained properly.
It is the user’s facility management’s responsibility to ensure that all personnel
working with toxic chemicals, gases, and vapors are given comprehensive
instruction in the process. This instruction includes information on relevant
health hazards; national, state and local regulations; methods for safe use; and
methods to detect escape of the agent.
It is the user’s facility management’s responsibility to ensure regular training of
all personnel concerned with the operation and maintenance of the equipment,
including emergency procedures for any toxic, flammable, or explosive material
released into the environment. Records of attendance at training are maintained,
and evidence of understanding demonstrated.
45 70-2011-5643-0 Issue Date: 10/2015

ANNEX B Worksheets
Site Planning Worksheet
Key: Wall
Supporting Column Electrical Receptacle
Doorway Work Areas
Intake Ventilation Duct Equipment being replaced (rough opening)
Exhaust Ventilation Duct Scale =
46 70-2011-5643-0 Issue Date: 10/2015

Equipment Location Worksheet

2
2 1 2 Abator
1
Stacking 1 XL
Rack Aerator GS5
Sterilizer GS8
Sterilizer 1 Power Input and EO Vent
2 Local Exhaust
Scale =
47 70-2011-5643-0 Issue Date: 10/2015

ANNEX C Site Readiness and Installation Verification Forms

Site Readiness Verification Form: 3M ™
Steri-Vac™ Sterilizer/Aerator GS Series
Facility Name:
Note: The following
form must be completed Address:
by the purchaser facility
prior to scheduling the City: State/Province:
installation support
Country: ZIP/Post Code:
service visit by 3M
Health Care service Contact Person:
personnel or authorized
3M service personnel. 3M Representative:
General
1. All national, state and local regulations related to the use of Ethylene Oxide have been obtained and reviewed, and the
Yes No
requirements met.
Electrical Supply
2. Enter the supply circuit current rating (15–20 amps). Amps
3. Minimum supply voltage is greater than 200 volts (200–240 VAC, 50/60 Hz single phase). Yes No
Enter supply voltage. Supply Voltage VAC
Compressed Air
4. The compressor is labeled to verify the air supply is clean, with a maximum allowable dirt particle size of 0.5 microns, and free
Yes No
of oil and is dry to 10°C (50°F) dew point at 38°C (100°F) ambient.
5. The supply pressure is 7.0 kg/cm2 (100 psig) minimum to 10.5 kg/cm2 (150 psig) maximum. Yes No
6. The air flow rate is 2.2 liters per second at 5.6 kg/cm2 (4.7 cubic feet per minute at 80 psig) per sterilizer/aerator based on
Yes No
100% duty cycle compressor.
7. The volume of the air tank is adequate to meet the demand of all equipment used by the same air compressor. Yes No
Venting
8. The vent line goes from the GS Series sterilizer to the outside atmosphere directly without being terminated into any existing
Yes No
recirculating air flow system or ventilation system.
9. The vent line is a hard drawn copper tube. Yes No
10. Enter the total linear length of the vent line from the GS Series sterilizer to the termination point on the outside of the building. m / ft. CIRCLE UNIT
10a. If the answer to Question 10 is greater than 91 m (300 ft), has the system been approved by 3M? Yes No N/A
11. Enter the outside diameter of the vent line. cm / in. CIRCLE UNIT
12. The vent line termination is located more than 7.6 m (25 ft.) from any possible sources of ignition or any openings to the building
Yes No
(e.g., doors, fresh air intakes, unsealed windows, pedestrian walkways).
13. The vent line is gas tight. Yes No
14. If the vent line a. The vent line is insulated to protect from freezing (where required). Yes No N/A
extends outside of b. There is a 180° downward bend at the end for the vent line if a vertical installation. Yes No N/A
the building: c. There is a 90° downward bend at the end for the vent line if a horizontal installation. Yes No N/A
Local Exhaust System (only applicable when the local exhaust hood is connected and operating)
15. The local exhaust system meets the air flow requirements stated in the exhaust ventilation specifications in the 3M Site
Yes No
Planning and Installation Guide.
16. The flow rate at the end of the facility exhaust duct at the sterilizer hood is from 59 to 66 L/sec (125 to 140 cfm) for a single
Yes No
door unit or 118 to 132 L/sec (250) to 280 cfm for a double door unit.
17. The ductwork material is impervious to EO (galvanized metal or SST). Yes No
18. The local exhaust system termination is located more than 7.6 m (25 ft.) from any openings to the building. Yes No
19. The exhaust hood blower is suitable for continuous operation and protected from adverse weather. Yes No
I certify that I have assessed the above conditions and all have been met.
Facility Representative (print): Date:
Facility Representative (signature):
48 70-2011-5643-0 Issue Date: 10/2015
Installation Verification Form: 3M ™

Steri-Vac™ Sterilizer/Aerator GS Series
Facility Name:
Address:
City: State/Province:
Country: ZIP/Post Code:
Contact Person:
3M Representative:
Compressed Air Line

1. The supply pressure is 7.0 kg/cm2 (100 psig) minimum to 10.5 kg/cm2 (150 psig) maximum. The compressor Yes No
maintains a flow rate of 2.2 liters per second at 5.6 kg/cm2 (4.7 cubic feet per minute at 80 psig) per sterilizer/aerator
based on 100% duty cycle.
2. The air supply is clean, dry to a dew point of 10°C (50°F), and free of oil. Yes No
3. Supplied air filters are installed in the supply line. Yes No
4. The air enters the filter through the port marked IN. Yes No
5. The supply line filters are accessible for maintenance. Yes No
6. A shutoff is installed upstream from the air filter so that air can be turned OFF for machine service. Yes No
7. An air pressure gauge is installed between the filters and the air inlet to the GS Series sterilizer. Yes No
Sterilizer/Aerator Location
8. A minimum clearance of 51 cm (20 in.) is maintained on all sides and the top of the GS Series sterilizer. If the answer to Yes No
this question is ‘No’, the answer to Q8a must be ‘Yes’.
8a. If answer to Q8, is ‘No’, can the GS Series sterilizer be moved? Yes No
8b. If the GS Series sterilizer is movable, is a stainless steel braided, flexible tubing used for the vent line? Yes No
8c. Is there a flexible line used on the air service so the GS Series sterilizer can be moved without disconnecting that Yes No
service?
9. The unit has been installed in an area free of flammable gases and liquids, other than ethylene oxide (EO). Yes No
10. The unit has been installed in an area with at least 10 air exchanges per hour. Yes No
11. Do you have documentation that confirms a minimum of 10 air exchanges per hour is available for the installed unit? Yes No
12. The room air flow pattern is directed away from the equipment operator. Yes No
Local Exhaust System (only applicable when the local exhaust hood is connected and operating)
13. The local exhaust system meets the air flow requirements stated in the exhaust ventilation specifications in the 3M Site Yes No
Planning and Installation Guide.
14. The flow rate at the end of the facility exhaust duct at the sterilizer hood is from 59 to 66 L/sec (125 to 140 cfm) for a Yes No
single door unit or 118 to 132 L/sec (250) to 280 cfm for a double door unit.
15. The ductwork material is impervious to EO (galvanized metal or SST). Yes No
16. The local exhaust system termination is located more than 7.6 m (25 ft.) from any openings to the building (e.g., doors, Yes No
fresh air intakes, unsealed windows, pedestrian walkways).
17. The exhaust hood blower is suitable for continuous operation and protected from adverse weather. Yes No
I certify that I have assessed the above conditions and all have been met.
Facility Representative (print): Date:
Facility Representative (signature):
49 70-2011-5643-0 Issue Date: 10/2015

ANNEX D 3M™ Steri-Gas™ EO Gas Cartridge Dilution Charts

The following Tables provide estimates of air concentrations of ethylene oxide (EO) if the identified 3M™ Steri-Gas™ EO Gas Cartridge should empty into a
room, and provide the time needed for a room ventilation system to reduce the EO concentrations to acceptable levels. These charts are based on rooms
with 10 air exchanges per hour.
3M™ Steri-Gas™ EO Gas Cartridge 4-100 3M™ Steri-Gas™ EO Gas Cartridge 8-170
Room EO Time to Room EO Time to

Room Room Room EO gas concentration Room Room Room EO gas concentration
reach reach
volume volume airflow weight volume volume airflow weight
after spill 0.5 ppm after spill 0.5 ppm
(ft3) (m3) (cfm) (g) (ft3) (m3) (cfm) (g)
(ppm) (minutes) (ppm) (minutes)
600 17 100 100 3270 53 600 17 100 170 5559 56
700 20 117 100 2803 52 700 20 117 170 4765 55
800 23 133 100 2452 51 800 23 133 170 4169 54
900 25 150 100 2180 50 900 25 150 170 3706 53
1000 28 167 100 1962 50 1000 28 167 170 3335 53
1500 42 250 100 1308 47 1500 42 250 170 2224 50
2000 57 333 100 981 45 2000 57 333 170 1668 49
2500 71 417 100 785 44 2500 71 417 170 1334 47
3000 85 500 100 654 43 3000 85 500 170 1112 46
3500 99 583 100 561 42 3500 99 583 170 953 45
4000 113 667 100 490 41 4000 113 667 170 834 45
4500 127 750 100 436 41 4500 127 750 170 741 44
5000 142 833 100 392 40 5000 142 833 170 667 43
5500 156 917 100 357 39 5500 156 917 170 606 43
6000 170 1000 100 327 39 6000 170 1000 170 556 42
6500 184 1083 100 302 38 6500 184 1083 170 513 42
7000 198 1167 100 280 38 7000 198 1167 170 476 41
7500 212 1250 100 262 38 7500 212 1250 170 445 41
8000 227 1333 100 245 37 8000 227 1333 170 417 40
8500 241 1417 100 231 37 8500 241 1417 170 392 40
Spill ppm = [(gas weight in mg) / (room volume in cu m)] * [(1 ppm / (1.80 mg/cu m)]
cfm = (room volume in cu ft) * (10 air exchanges per hour) / (60 min/hr)
time = [log10(0.5 ppm / spill-ppm)] * [(-2.303) * (room volume in cu m) / (cfm)]
Employee monitoring may be required by national, state and local regulations. In the U.S., the Occupational Safety and Health Administration (OSHA)
requires breathing zone monitoring of employees for exposure to ethylene oxide after the 3M™ Steri-Vac™ GS Series Sterilizer/Aerator GS Series installation
to establish a baseline (OSHA 29 CFR 1910.1047). The 3M™ Ethylene Oxide (EO) Monitoring Badge 3550 can be used to facilitate personal monitoring
compliance to the OSHA standard.
3M™ Steri-Gas™ EO Gas Cartridge Safety Data Sheets (SDS) are available at: www.3M.com/msds
50 70-2011-5643-0 Issue Date: 10/2015

ANNEX E Bibliography and Compliance References

Equipment and Ethylene Oxide (EO) Compliance Documents
Biological evaluation of medical devices – Part 7: EMC Directive

AAMI/ISO 10993-7 2004/104/EC Electromagnetic Compatibility
Ethylene oxide sterilization residues
Sterilization of health care products – Ethylene Sterilizer/Aerators for Medical Purposes – Ethylene
oxide – Part 1: Requirements for development, EN 1422 Oxide Sterilizer/Aerators – Requirements and Test
AAMI/ISO 11135-1 Methods
validation, and routine control of a sterilization
process for medical devices.
EN 62366 Medical Devices – Application of usability
Automatic, general purpose ethylene oxide engineering to medical devices
ANSI/AAMI ST24 Sterilizer/Aerators and ethylene oxide sterilant
sources intended for use in health care facilities National Emission Standards for Hazardous
EPA 40 CFR Part 63; Air Pollutants for Source Categories – National
Subpart WWWWW Emission Standards for Hospital Ethylene Oxide
ANSI/AAMI ST41 Ethylene oxide sterilization in health care Sterilizer/Aerators
facilities: Safety and effectiveness
FCC part 15 Electromagnetic Compatibility
ANSI/AAMI/IEC Application of risk management for IT Networks
80001-1:2010 incorporating medical devices – Part 1: Roles,
responsibilities and activities Safety requirements for electrical equipment for
IEC/EN 61010-1 measurement, control, and laboratory use – Part
1: General Requirements
ANSI/AAMI/ISO Medical device software – Software life cycle
62304 processes Safety requirements for electrical equipment for
IEC/EN 61010-2-010 measurement, control and laboratory use – Part
2-010: Particular requirements for laboratory
AOAC Official Method of Analysis of Official equipment for the heating of materials
AOAC Analytical Chemist (AOAC), 14th Ed., Chapter 4,
Disinfectants, Par. 4.033-4.035. Safety requirements for electrical equipment for
measurement, control and laboratory use – Part
IEC/EN 61010-2-040 2-040: Particular requirements for Sterilizer/
American Society of Heating, Refrigerating, and Aerators and washer-disinfectors used to treat
Air-Conditioning Engineers. Ventilation of health medical materials.
ASHRAE
care facilities. ANSI/ASHRAE Standard 170.
Atlanta: ASHRAE, 2008. Biological evaluation of medical devices – Part
ISO 10993-17 17: Establishment of allowable limits for leachable
substances
American Society of Heating, Refrigerating, and
ASHRAE; 201.4 Air-Conditioning Engineers. HVAC Design Manual “Sterilant Use of EO in Hospitals & Health
for Hospitals and Clinics; 2nd ed. Atlanta, GA. Care Facilities,” ANNEX A, Table VII; OSHA EO
ASHRAE; 201.4 OSHA 29 CFR 1910
Standard: 29 CFR 1910 Occupational Exposure
to Ethylene Oxide.
Australian Standard Limits and methods of measurement of
for EMC – electronic disturbance characteristics of OSHA 29 CFR General Industry Standard Subpart Z (Toxic and
AS/NZS 2064 industrial scientific and medical (ISM) 1910.1047 Hazardous Substances; Ethylene Oxide)
radiofrequency equipment.
ANNEX F Disposal of Packaging

Recycle packaging materials according to facility policy. Dispose of non-recycled packaging materials into general waste or according to facility policy.
51 70-2011-5643-0 Issue Date: 10/2015

Contact Information
For additional information on installation, seismic bracing, accessories,
preventive maintenance agreements, services or other questions,
contact 3M at the sites listed below or your local 3M office.
3M Health Care
3M Health Care Service Center
Building 502-1W-01
St. Paul, MN 55128
1-800-292-6298
www.3m.com/infectionprevention
3M Canada, Inc.
P.O. Box 5757
London, Ontario,
Canada, N6A4T1
1-800-563-2921
3M Deutschland GmbH
Health Care Business
Carl-Schurz-Str.-1
41453 Neuss, Germany
3M
3M Health Care
Infection Prevention Division
3M Center, Building 275-4E-01
St. Paul, MN 55144-1000 Please recycle. Printed in USA.
USA © 3M 2015. All rights reserved. 3M, Steri-Gas and Steri-Vac are trademarks of 3M Company.
1-800 228 3957 Issued 10/15. 10896HB SECURALL, Arrow Dryers, Grainger and Powerex, Inc. are all
www.3M.com/infectionprevention 70-2011-5643-0 Rev. B trademarks of their respective companies.

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3M™ Steri-Vac™ Sterilizer/Aerator GS Series

Ventilation Failure Detector........................................................................... 23 Equipment Location Worksheet .....................................................................47

2 70-2011-5643-0 Issue Date: 10/2015

Device Safety Compliance

3 70-2011-5643-0 Issue Date: 10/2015

4 70-2011-5643-0 Issue Date: 10/2015

Step 3 Prepare the Area and Service Requirements

Step 4 Install the Equipment

5 70-2011-5643-0 Issue Date: 10/2015

II. Select the Equipment

78-8055-6040-2 Stainless lower basket 39 × 80 × 18 cm (15.5 × 31.5 × 7 in)

78-8078-8313-3 Stainless steel lower basket 47 × 95 × 20 cm (18.5 × 37.5 × 8 in)

6 70-2011-5643-0 Issue Date: 10/2015

Figure 1. 3M™ Steri-Vac™ Sterilizer/Aerator GS Series, Model GS5

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Figure 2. 3M™ Steri-Vac™ Sterilizer/Aerator GS Series, Model GS8 Single Door

Side Elevation Front Elevation

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III. Select the Location

Environmental Condition Condition Range Units

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Acceptable Air Flow Unacceptable Air Flow

"Dead" Air Space

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Site Planning Worksheet

Figure 4. Site Planning Example

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Proposed Location of Equipment

Figure 5. Work Area and Equipment Location Example

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Figure 7. Typical In-Wall Opening Requirements for 3M™ Steri-Vac™ Sterilizer/

111.8 cm (44 in.) Max.

Pre-Installation Visit and Site Readiness Verification

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IV. Preparing the Area and Service Requirements

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Electrical Service Requirements

Table 3 – Electrical Service Requirements

UL listed to U.S. and Canadian Safety Standards

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Compressed Air Requirements

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Multiple Sterilizer/Aerator Installations

Compressed Air Line Installation Kit

7' High Pressure

⁄ " NPT Bushing

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Ethylene Oxide Vent Line Requirements

3M Abator (Emission Control Devices)

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Vent Line Labeling and Install Considerations

Figure 10. Ethylene Oxide Vent Line Connection Details

⁄ " NPT, 2" Long Nipple

3 ⁄4" SWT to 1" Copper Line

⁄ " NPT to 3⁄4" SWT

7' Flexible Vent Line

⁄ " NPT Union

⁄ " NPT Elbow

Figure 11. Ethylene Oxide Horizontal Vent Line Installation Example