3
11
Functional Verification
This procedure helps to confirm the proper operation of the Micropaq monitor. No monitor
disassembly is required.
The following equipment is required:
Visual Check
Perform this check if the monitor is being serviced in the field by a biomedical/clinical
engineer.
1.
Verify that the rubber gasket is not protruding from the case.
2.
Verify that the rubber feet have been installed.
3.
Verify that screw covers are in place over all four screws in the battery compartment
and the small recessed connector next to the battery connector.
4.
Verify that the correct labels have been applied to the case. (See
on page 48 for Model 404 monitors or
on page 60 for Model 402
monitors.)
a.
Verify that the correct rear case label and battery label are attached.
b.
Verify that the serial number label is attached and that the correct information has
been recorded for the model number, part number and serial number.
c.
Verify that the clear label cover has been applied over the serial number label.
Model
Required Equipment
402 and 404
•
DNI Nevada Inc. Patient Simulator 217A or 214B (or equivalent ECG patient simulator)
•
Micropaq ECG Cable (008-0522-XX)
•
Fully charged battery
•
Access to a properly functioning FlexNet network with an access point within range
404 with Masimo •
Micropaq Masimo SpO2 cable (008-0961-XX)
•
Masimo adult SpO2 sensor for finger
•
BIO-TEK Index 2 Series SpO2 Simulator with optical finger for sensor connection (or equivalent)
404 with Nellcor
•
Micropaq Nellcor SpO2 cable (008-0754-XX)
•
Nellcor adult SpO2 sensor for finger
•
BIO-TEK Index 2 Series SpO2 Simulator with optical finger for sensor connection (or equivalent)
