Penlon · Model Vapor
The Penlon Vapor is one of the premier anesthesia gas machines.
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: Delivered agent concentration off, low/high agent alarm.
Root cause: Worn bellows or O-ring; agent contamination.
Symptoms: O2 low-pressure alarm, inability to ventilate.
Root cause: Pipeline disconnect or failed O2 flush valve.
Symptoms: Low minute volume, volume loss, leak alarm.
Root cause: Loose connections, torn bellows, cracked hose.
Symptoms: Rising EtCO2, patient rebreathing.
Root cause: CO2 absorbent saturated.
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, replace on schedule.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Breathing circuit / bellows | Periodic replacement | $$ | Fairly easy |
| CO2 absorber canister Consumable, replace on schedule. | Consumable | $ | Easy |
| Scavenger interface & hose | Periodic replacement | $$ | Fairly easy |
| O2 pressure regulator | 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.
Synced live from the FDA openFDA API.
It has come to Penlon Ltd's attention of an instance where the installation and pre-use checks listed in the User Manual may not have been followed prior to the clinical use of the vaporizer. Penlon Ltd has updated the Installation and daily Pre-Use Check sections of the User Manual to ensure that the instructions are explicit and clear.
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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