Datascope · Model Passport V
A comprehensive range of options that make it well-suited for most hospital departments The flexible feature-set includes your choice of CO 2 and SpO2 technologies. Additional offerings such as multiple invasive pressures, external device interfacing and a secondary display solution are also available for increased monitoring of your more critical patients.
Failure patterns typical of this equipment class - general BMET reference, not verified against this exact unit's own service history unless flagged. Severity is a category-level estimate.
Symptoms: Flat or noisy ECG, frequent lead-off alarms.
Root cause: Worn electrodes, loose leads, or dry gel.
Symptoms: No pleth, SpO2 drops to --- or false low.
Root cause: LED/photodiode aging or cable damage.
Symptoms: Short backup time, battery alarm on transport.
Root cause: Aged backup battery.
Symptoms: Dim, flickering, or unresponsive screen.
Root cause: Backlight or digitizer failure.
The parts a BMET typically services on this class of equipment. Service class and relative cost are general engineering estimates for the category, not figures from this unit's documentation. Part numbers appear only when pulled from this unit's own service manual. Always confirm intervals and pricing against the manufacturer.
Consumable per patient.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| SpO2 sensor (adult/ped/neo) | Frequent wear item | $$ | Easy |
| NIBP cuff & hose Consumable per patient. | Periodic replacement | $ | Easy |
| Rechargeable backup battery | Periodic replacement | $$ | Fairly easy |
| Display / touch assembly | Periodic replacement | $$$ | Difficult |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
Preventive-maintenance tasks typical of this equipment class. Perform to the manufacturer's procedure and your facility's policy - this is general reference, not a schedule for this specific unit.
A structured starting point derived from the failure modes above. Follow the manufacturer's service documentation for the actual procedure.
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
No documents available for this device yet.
Synced live from the FDA openFDA API.
Potential inaccurate printed information in the upper and lower margins of a print strip.
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
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