Dräger Narkomed 2B Service Manual page 179

NM2B
PM Certification Procedure for Narkomed 2B Anesthesia System
Place a "CAUTION DO NOT USE" label (part # 4114327) on the vaporizer, and issue a
departmental alert. The TSR shall also seek permission from the equipment operator to remove
the failed vaporizer from the machine and install a replacement vaporizer or an adapter block
onto the mount. All nonfunctional Dräger vapor vaporizers must be removed from service for the
machine to receive certification.
10. Proceed with PM Certification procedure. If any tests fail refer to the "Failure Codes" listing in
DMI Recommendations Guidelines Index (P/N S010250) to determine correct certification level
starting point. Failure codes shall be documented on the "RECOMMENDATIONS / GENERAL
COMMENTS" section of the PM Certification form and on the Executive Summary. If a test fails
that has not been identified by the "Failure Codes" list, consult with DMI Inc. to assess the
proper certification level.
11. Based on the
RECOMMENDATIONS" that would apply. Use the Narkomed 2B section of the
"RECOMMENDATION GUIDELINES INDEX" (P/N S010250). Note all applicable DMI
recommendations on the Executive Summary. NOTE: If using a carbon form, indicate the
Equipment Condition number and to see reverse side under the "RECOMMENDATIONS /
GENERAL COMMENTS" section of the form.
12. Determine the correct certification level of the machine based on the combined lowest common
denominator of "Equipment Conditions" and "Failure Codes". If the machine is at least
conditionally certified fill out the "PM CERTIFICATION" label. Check the box(s) on the
validation label where appropriate. Write the month and year, (three months from date of PM
Certification) next to "NEXT VISIT DUE:" If certification level is "D", machine shall not receive
a "PM CERTIFICATION" label. Any machine not receiving a PM Certification label shall receive
a "WARNING NOT CERTIFIED" label. This label shall be placed at a prominent location on the
left side of the machine after all other previous PMS and Vigilance Audit Validation labels have
been removed.
13. In the "CERTIFICATION LEVEL" section of the PM Certification form, record the last visit
certification level, the current certification level and the next visit due month and year, (three
months from date of PM Certification) in the spaces provided.
14. If applicable, remove the previous PM CERTIFICATION VALIDATION label and attach the new
label (P/N S010006 w/phone #, or P/N S010007 w/o phone #) in a prominent location on the rear
of the anesthesia machine.
15. Check the appropriate boxes on the "PM CERTIFICATION NOTICE" label, (part # S010011).
If the machine is not certified, the last box of this notice label shall be marked. Attach this
notice to the flow shield of the anesthesia machine.
16. Have the customer sign each PM Certification form or the Executive Summary, and review the
equipment conditions and the recommendations with the customer.
17. Return top copy to Draeger Medical, Inc. Service Department, keep middle copy for service
organization records, give bottom copy to customer.
Rev. Y
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"EQUIPMENT CONDITION"
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PMC PROCEDURE (continued)
inspect the machine for any "DMI