Midmark M9-040 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

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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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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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.

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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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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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003-2915-99

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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003-2915-99

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

English - 13

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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.

*

English - 14

003-2915-99

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.

English - 15

003-2915-99

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.

English - 16

003-2915-99

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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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...

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 

  

 

  

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 M9-040 Manuel utilisateur

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