Midmark M9-041 Manuel utilisateur

Taper
Manuel utilisateur
003-2915-99 Rev AA7 (12/4/18)
TP202 20-42-FO-00014 Rev A1 C2169
Style U
TP202 20-42-FO-00014 Rev A1 C2169 TP202 20-42-FO-00014 Rev A1 C2169
M9 / M9D / M11
Self -Contained Steam Sterilizer
For Models:
M9 (-040 / -041 / -042)
M9D (-042)
M11 (-040 / -041 / -042)
User Guide
English
Español
Français
English - 2
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© Midmark Corporation 2018
003-2915-99
Model / Serial Number:
Date of Purchase:
Authorized Service Company:
Dealer :
Product Information
Serial Number
Model / Serial
Number Label
English - 3
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© Midmark Corporation 2018
Table of Contents
Important Information
Safety Instructions ...........................................4
Intended Use....................................................4
Sterilization Technology ...................................4
Electromagnetic Interference ...........................4
Safety Symbols ................................................4
Shipping Symbols ............................................5
Transportation / Storage Conditions ................5
Accessories, Tools and Service Parts. ............. 5
Included with Sterilizer .....................................6
Component Location ........................................ 7
Controls and Indicators ....................................8
Sterilization Monitoring Guidelines.................10
Installation
Operating Environment .................................. 11
Location Requirements .................................. 11
Electrical Requirements .................................12
Connecting the Power Cord ........................... 13
User Settings .................................................14
Operation
Before Operating the Sterilizer.......................15
Filling the Reservoir .......................................15
Qualication Testing ....................................... 16
Guidelines for Loading ...................................16
Standard Cycle Parameters ........................... 24
Cycle Operation .............................................25
Post-Sterilization Processing .........................28
Programmable Cycle Buttons ........................29
Maintenance
Maintenance Messages .................................31
Daily Maintenance .........................................32
Weekly Maintenance ......................................33
Monthly Maintenance ..................................... 35
Extended Use Maintenance ........................... 37
Thermal Printer (Optional)
Operating the Printer......................................38
Printer Tape Description ................................38
Example of Typical Printout
of a Program Cycle ........................................39
Paper Roll Removal / Installation ................... 40
Tray and Cassette Tool (optional)
Using the Optional Tray / Cassette Tool.........41
Troubleshooting
Troubleshooting Chart ....................................42
Informational Messages ................................. 43
Accessing the last 5 Error Codes ..................43
Error Messages..............................................43
Calling for Service .......................................... 45
Specications / Compliance
Specications Chart:
M9 / M9D .................................................46
M11 .........................................................47
Water Purity Specications ............................48
Warranty Information
Scope of Warranty .........................................49
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© Midmark Corporation 2018
Important Information
Safety Instructions
The primary concern of Midmark is that this equipment is operated and maintained with the safety of the
patient and staff in mind. To assure safe and reliable operation:


(This is the responsibility of the purchaser).

to the sterilizer.
Intended Use


Guidelines
for loading and Standard Cycle Parameters in this manual for detailed information.
Sterilization Technology
The Midmark M9 / M9D and M11 utilize a dynamic air removal system called Steam Flush Pressure Pulse to
remove air from the chamber.
Electromagnetic Interference

interference is noticed between another device and this product:
 
 
 
 
Safety Symbols
WARNING
Indicates a potentially hazardous situation which could result in serious injury.
Caution
Indicates a potentially hazardous situation which may result in minor or moderate injury.
It may also be used to alert against unsafe practices
Equipment Alert
Indicates a potentially hazardous situation which could result in equipment damage.
English - 5
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© Midmark Corporation 2018
Shipping Symbols
Proper shipping orientation
Fragile
Caution Shipping Damage

(Refer to “n” number on package)
Keep dry
Accessories, Tools and Service Parts

Common Service Parts / Tools Order Number
Printer Thermal Paper Roll (Rell) 060-0016-00
Printer Stick-able Thermal Paper (Rell) 060-0016-01
Door and Dam Gasket Kit (M11 only) 002-0504-00
Door and Dam Gasket Kit (M9 / M9D only) 002-0361-01
Pouch Rack Kit (M11 only) 002-2108-00
Pouch Rack Kit (M9 / M9D only) 002-2108-01
Tray/Cassette Tool 9A307001
VistaCool ™ direct-to-drain thermal reduction system 9A586002 (Dual)
Transportation / Storage Conditions
Equipment Alert
Water must be drained from the unit’s reservoir before transporting / storing below +32°F (0°C).
Ambient Temperature Range: -22°F to 140°F (-30°C to +60°C)
Relative Humidity: 10% to 90% (non-condensing)
Atmospheric Pressure: 7.2 psia to 15.4 psia (49.6 kPa to 106.4 kPa)
Accessories Order Number
Speed-Clean, 1 (16oz. [.47 liter]) bottle 002-0396-00
Speed-Clean, 1 case (12 - 16oz. [.47 liter]) bottles 002-0396-05
Thermal Printer 9A599001
Cassette Rack (Horizontal) 9A215001 (M11 only)
Cassette Rack (Vertical) 9A215002 (M11 only)
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© Midmark Corporation 2018
Included with Sterilizer
Pouch Rack
(M11 Rack Shown)
Speed-Clean
2 Small Trays
2 Large Trays
Speed-Clean SDS SheetCare / Operation Card
Power Cord
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Component Location
Pressure Relief
Valve Test Lever
Thermal Printer
(optional)
Display / Touch Pad
Tray Rack
Door Gasket
Dam Gasket
Tray(s)
Water Level Indicator /
Reservoir Drain Tube
Tray Plate
Fill Opening
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Controls and Indicators

The accompanying tables describe the function of each control / indicator.
Control Function
Display See illustration 


remaining cycle time is displayed as well as temperature and
pressure. Display also shows error message if a malfunction
Troubleshooting section of this manual for a
 Informational / Error Messages.
Unwrapped button

270°F (132°C) for 3:00 minutes / 30 minute drying cycle.
Pouches button

paper / plastic sterilization pouches or wrapped instruments
at: 270°F (132°C) for 4 minutes / 30 minute drying cycle.
Packs button

250°F (121°C) for 30 minutes / 30 minute drying
cycle.
Handpieces
button

270°F (132°C) for 4 minutes / 30 minute drying cycle.
Start button

pressing Start will activate heater for 10 minutes.
Stop button
Terminates selected program or function.
1 or 2 buttons

run in these cycles
must be validated
for sterilization by
the user.
Programmable cycle buttons that allow an operator to create two
different programmed cycles for special applications. Sterilization
-
dure can be adjusted or changed.
Caution
These cycles are not FDA cleared and validation of sterility
of items processed using them is the responsibility of the
user.
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Controls and Indicators - continued...
Control Function
P button Programming mode button that allows operator to

procedure. Used in conjunction with buttons 1 or 2.

+ (plus) button

be increased or changed when in location 1 or 2
and the P (programming) mode is activated.
- (minus) button

be decreased or changed when in location 1 or 2
and the P (programming) mode is activated.
Door Handle refer to illustration For latching / opening door.

 refer to illustration
Shows amount of water in reservoir. Tube also
used for drainage of reservoir into suitable
container.
Fill Opening refer to illustration 
 refer to illustration 
Thermal Printer (Optional) refer to illustration The printer (optional equipment) can be used to

and pressure during a cycle.
Fill Opening
Water Level Indicator and
Reservoir Drain Tube
Door Handle
Thermal Printer
(optional)
Pressure Relief
Valve Test Lever
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Sterilization Monitoring Guidelines
Physical Monitors
Temperature and pressure measuring devices can help detect sterilizer malfunctions. The sterilizer’s control
system aborts the cycle and displays a message if physical conditions go outside established limits. The

pressure.
Chemical Indicators
Chemical indicators are designed to verify that conditions in the sterilizer chamber were adequate to achieve

items in that load are considered non-sterile. Potential causes for sterilization failure include: improper



Sterilizers should be used for monitoring the cycles. Follow the chemical indicator’s instructions for proper

Biological Indicators
Biological indicators are microbiological devices designed to accompany items being sterilized to monitor






disposal.
Note
This information below is provided for reference only. Contact appropriate state/local agencies for
specific sterilization guidelines for your office. Additional information on infection control is available
from the Centers for Disease Control and Prevention (CDC), Organization for Safety and Asepsis
Procedures (OSAP) ), Association for the Advancement of Medical Instrumentation (AAMI), and
Association for Professionals in Infection Control and Epidemiology (APIC).
Note
Use only FDA cleared chemical and biological indicators designed for steam sterilization that are
compatible with the particular sterilization cycle temperature and exposure time being monitored.
Use sterility monitors with each sterilization load. If a sterilizing cycle is terminated prematurely,
reprocess instruments to ensure sterility of the load. Follow manufacturer’s instructions for proper
disposal of used indicators.
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2"
(5 cm)
Clearance
21"
(53 cm)
Support Surface
1"
(3 cm)
5"
(13 cm)
Requirements
5"
(13 cm)
18"
(46 cm)
M11
M9/M9D
M11
23" (58 cm)
M9/M9D
22" (56)
2"
(5 cm)
Overhang/Shelf
M9/M9D
18"
(46 cm)
M11
15"
(38 cm)
Installation
Operating Environment
Ambient Temperature Range: 68°F to 104°F (+20°C to +40°C)
Relative Humidity: < 80% (non-condensing)
(Pollution Degree 2, in accordance to IEC664)
Normal Operating Altitude: < 9842 ft. (3000 m) above sea level
Device approved for INDOOR USE ONLY.
Device to be operated in a relatively dust-free environment.
(Pollution Degree 2, in accordance to IEC664)
Device should be connected to a power source with over-voltage limits less than 1500 watts from
mains to ground. (Installation Category II in accordance to IEC664)
The M9 / M9D and M11 will emit 5000 BTU / HR during operation.
Location Requirements
Allow Clearance
on Both Sides
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Location Requirements - continued...
Support Surface


 

Dimensions
Depth (front to back) M11 - 21” (53 cm) M9 / M9D - 18” (46 cm)
Clearance Requirements



the surrounding area.
Back of Unit - Back Wall ................................. 2” (5 cm)
Front Support Surface - Front Sterilizer ........ 1” (3 cm)
Sides of Unit - Side Wall ................................ 2” (5 cm)
 .......... 5” (13 cm)
 ..... M11 - 18” (46 cm) M9 / M9D - 15” (38 cm)
Under Cabinet or Shelf................................... M11 - 23” (58 cm) M9 / M9D - 22” (56 cm)
Relocation Requirements for Sterilizer
Disconnect power cord from electrical outlet and allow sterilizer to cool.

WARNING
For 115 VAC models: Use 104 - 127 VAC, 50/60 Hz alternating current only.
For 230 VAC models: Use 207 - 253 VAC, 50/60 Hz alternating current only.
Failure to do so may result in electric shock to personnel and / or damage to sterilizer.
Note
For safety, the unit must be connected to a properly polarized and grounded receptacle. Always use a
power cord with grounding connections that match the receptacles in your location.
115 VAC Unit: 


230 VAC Unit: 


* Power source must have over-voltage limits less than 1500 watts from mains to ground.
(Installation Category II in accordance to IEC664)
Electrical Requirements
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Display:
WARNING
Check the serial number label on back panel of sterilizer to verify voltage rating for
the unit. Failure to connect sterilizer to an appropriate power supply could result in
damage to the unit, and electrical shock to personnel.
Voltage Rating
Connecting the Power Cord
Equipment Alert
For optimal performance, allow sterilizer to reach room temperature before operating.
To connect the power cord...
A) Plug power cord into receptacle on back of sterilizer.
B) Plug power cord into a properly polarized and grounded receptacle rated for a
minimum of 15 amps. A dedicated circuit only used for the sterilizer is recommended.
C) M9 / M9D and M11 are not equipped with an on/off switch, the display operates off
very low power. (example: microwave oven display)
Note: When power is connected, the messages shown below will appear on the display.
WARNING
Equipment is not suitable for use in the presence of a flammable anesthetic mixture
with oxygen, air, or nitrous oxide.
Clarification: Equipment is suitable for use in the presence of oxygen, air, or nitrous oxide.
*
* These screens will display the total number of cycles run on the unit, the model number
(M9 / M9D or M11), the software version number, serial number date, and time.
*
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© Midmark Corporation 2018
Action Description Display
Press Press start to initialize the User Settings
menus.
Adjust Units of
Measure
The “+” and “-” buttons alternate the
setting between English or Metric
When the desired Units of Measure
appear on the display...
Press
To store the desired Units of Measure
This brings up the Time Clock programing
display
Adjust Time Clock The “+“ and “-” buttons will adjust the
values of the following settings

Minute.
When the desired values appear on the
display...
Press 

for all settings. When all settings are
completed pressing the “P” will initiate
normal power up.
NOTE: User Settings for Date and Clock must be updated manually for day light savings and leap year
User Settings
User setting mode will enable the user to set the desired unit of measure and adjust the time
clock. To enter the user settings mode, unplug and replug the power cord while pressing and
holding the button until the User Settings screen below appears.
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Operation
Before Operating the Sterilizer
Filling the Reservoir
Caution
Programmable cycles 1 and 2 are provided for those applications requiring sterilization
parameters different than the preset cycles. These cycles are not FDA cleared for medical
use. All material processed in these cycles must be validated by the user to ensure sterility of the
processed load.
WARNING
Do not use this sterilizer for sterilizing volatile substances or for any purpose other
than its intended design. Burns and toxic or explosive conditions could result.
Do not force door handle at any time. Chamber pressure may cause door to open with
extreme force. If door handle does not move freely, allow unit to cool and depressurize for 40
minutes before opening door. Failure to adhere could result in serious personal injury.
Do not run the sterilizer without the tray plate in place. If the sterilizer malfunctions,
immediately unplug sterilizer, and call for service; do not attempt to repair the sterilizer
yourself. Doing so could result in serious injury.
Equipment Alert
For optimal performance, allow the sterilizer to reach room temperature before operating.
To fill reservoir...
A) Open door to unit.
B) Pour distilled water into fill opening until
water level reaches the top of the fill level
label on the water level indicator tube.
Equipment Alert
Use distilled water or water that meets the
referenced water purity specifications.
Failure to comply may result in sterilizer
malfunction and/or premature failure due
to excessive corrosion.
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Guidelines for Loading
Qualication Testing













the biological testing for all three test runs are available.
Equipment Alert







be followed.”
Types of Items that can be processed in the M9 / M9D and M11

the

The M9 / M9D and M11 are designed to sterilize the following:
 
 (ex. suction cannulas, impression trays, etc.)
 (ex. CSR wrap, instrument pouches, etc.)
 
 
 (ex. opthalmologic instruments)
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Preparing Items for Sterilization


manufacturer’s instructions for proper cleaning and preparation of the device for sterilization should always
be followed:


recommended over manual cleaning for clinician safety and cleaning effectiveness.




packaging.


Immediate Use Sterilization
The M9 / M9D and M11 are capable of Immediate Use sterilization - sterilizing unwrapped instruments for


another (See Photo 1).
WARNING
Clean and dry instruments thoroughly before placing them into tray. Improper cleaning may
result in non-sterile instruments or damage to the unit. Follow instrument manufacturer’s
guidelines and CDC recommendations for handling and cleaning instruments prior to sterilization.
Equipment Alert
Do not sterilize items composed of any of the following materials in the M9 / M9D or M11.
• Corrosion sensitive metal (ex. carbon steel, iron, etc.)
• Fragile items susceptible to breaking under pressure / high temperature
• Biomedical waste
• Plastics that may break down or produce residue when exposed to steam / high
temperatures.
Examples


Types of Items that can be processed in the M9 / M9D and M11 - Continued...
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Photo 1
Please consider the following when choosing whether or not to sterilize your instruments unwrapped:






these procedures on a routine basis
WARNING
Do not overload the chamber! Adequate space is required around items in trays for
steam circulation and drying. Failure to allow adequate space will compromise
sterilization and drying. Items and packaging should be completely dry when removed from
the sterilizer to minimize the potential for recontamination.
General Guidelines



must not scrape the chamber walls when sliding the tray into the chamber.

(See Photo 2).
Immediate Use Sterilization - Continued...
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© Midmark Corporation 2018
Photo 2



positioned on the tray with the open side down so any water condensate drains from the
container (See Photo 3). When sterilizing glassware check with the manufacturer to make sure
it is compatible with steam sterilization.


the tubing ends are open and unobstructed (See Photo 4).
Photo 3
Photo 4
General Guidelines - Continued...
English - 20
003-2915-99
© Midmark Corporation 2018




recontamination.

operator to increase the default drying time to assure all packaging and instruments are
completely dry. See “Cycle Operation” section of this manual for instructions on adjusting drying
time.

Pouches or Unwrapped Cycle.
Pouching and Wrapping Items
The M9 / M9D and M11 are capable of sterilizing pouched or wrapped items to preserve sterility
after processing.


manufacturer’s instructions for use.



steam circulation and avoid potential instrument damage.




additional dry time may be required.


the pouches should be oriented in the rack so the plastic side of one pouch faces the paper side
of the adjacent pouch.



penetration to the items (See Photo 2).
M11 Pouch Rack
002-2108-00
M9 / M9D Pouch Rack
002-2108-01
General Guidelines - Continued...
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Midmark M9-041 Manuel utilisateur

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