NMGS
PMC PROCEDURE (continued)
6-9
PM Certification Procedure for Narkomed GS Anesthesia System
1.
Use the PM Certification form for Narkomed 2B/ 2C/ GS Anesthesia Systems (P/N
S010211).
2.
Completely fill in the header information.
1.
All Narkomed GS are equipped with Humphrey valves and do not require
lubrication. Indicate so with a (H) next to the “Vent Valve Lube Due” line on the
Periodic Manufacturer’s Certification form.
2.
Replace the VENTILATOR RELIEF VALVE DIAPHRAGM every 12 months in
accordance with SP00075. Place a check mark and indicate the next replacement
date at “Relief Valve Diaphragm Due” line on the Periodic Manufacturer’s
Certification form.
5.
If machine is equipped with a HALOTHANE Dräger Vapor 19 or 19.1 vaporizer,
determine if vaporizer must be inspected for soil condition one. Check the serial
number plate located on the rear of the vaporizer for a plus (+) preceding the serial
number. A HALOTHANE vaporizer serial number not preceded with a (+) must be
tested for soil in accordance with SP00073. If vaporizer does not need to be inspected,
indicate so with a plus (+) next to the “Vapor Inspection (H)” line on the Vigilance
Audit form. If vaporizer is soil condition 0, indicate so with “SOIL 0” written next to
the “Vapor Inspection (H)” line on the Vigilance Audit form. If vaporizer is soil
condition one, indicate so with “SOIL 1” written next to the “Vapor Inspection (H)”
line on the Vigilance Audit form. 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 apply a replacement vaporizer or an adapter block onto the mount. All
“SOIL 1” vaporizers must be removed from service for machine to receive
certification.
6.
Perform the vapor concentration test on all Dräger vapor vaporizers in accordance
with SP00073 at a six month maximum interval. Perform the vaporizer concentration
test on all Desflurane vaporizers in accordance with SP00091 for fixed mount
vaporizers and SP00189 for user removable D-tec vaporizers at a six month
maximum interval. For every vaporizer tested, fill out a “VAPOR VAPORIZER
CALIBRATION CHECK” label (part # S010016). Information on this label shall
include your signature, type of agent, date tested, a No Agent To Test or the test
results @ 1%, 2.5%, 4% for H, E, I, or S vaporizers, or @ 4%, 10%, 12%, 16% for
Desflurane vaporizers, and a PASS or FAIL indication. This label shall be attached to
the upper right side of the vaporizer. If vaporizer fails the concentration verification,
internal leak, or exclusion system tests, check “NO” in the “RECOMMENDED FOR
USE” section on the PM Certification form. 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 customer to remove the failed vaporizer from the machine
and install a replacement vaporizer or an adapter block onto the mount. All
nonfunctional vaporizers must be removed from service for machine to receive
certification.
Содержание Narkomed GS
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