Osypka · Model Pace 203 H
Rounded design, small size, and low weight of pacemaker Easy and quick operation with knobs and push buttons Automatic functions for AV-Delay, PVARP, MTR and sensitivity Atrial Trigger also in DDD mode Electrode surveillance for short circuit and interruption Display illumination (can be switched off optionally) Safe against cross talk and defi shocks Settings can be saved
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: Charge fails or sluggish, low-energy delivery.
Root cause: Capacitor aging / leakage.
Symptoms: No shock delivered, pad error.
Root cause: Worn paddles or expired pads.
Symptoms: Won't charge or discharges unexpectedly.
Root cause: Relay/contactor wear.
Symptoms: Leakage alarm, self-test fail.
Root cause: Failed isolation components.
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.
Critical - keep charged spares.
Expiration-dated consumable.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Rechargeable battery pack Critical - keep charged spares. | Periodic replacement | $$$ | Fairly easy |
| HV energy storage capacitor | Major service part | $$$$ | Expert-level |
| Defibrillation electrodes / pads Expiration-dated consumable. | Consumable | $$ | Easy |
| Charge relay / contactor | 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.
The recall was initiated after Osypka Medical received two (2) complaints from their Japanese distributor regarding an incompatibility of the PACE 203H with some new types of 9 V batteries. The investigation revealed that PACE 203H of a certain manufacturing period malfunction (i.e., not stimulate) when a type of 9 V batteries with higher than usual open circuit voltage (OCV) is used. Failure t
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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