Dräger · Model Isolette C2000
Infant Incubator An advanced thermoregulation system, controlled by Dräger’s elaborate PID algorithm, keeps the baby in a stable environment. Very low velocity is used to create a calm zone that surrounds the neonate, inhibiting convective heat loss, while dual air curtains and preemptive regulation mechanisms maintain practically stable conditions during access to the infant. The servo-controlled humidifier provides optimal comfort levels and helps to prevent the excessive transepidermal water and concomitant evaporative heat loss common to the first days of neonatal life. The double wall design further maximizes heat conservation. The superior thermoregulation features found in the Isolette® C2000 help infants thrive. Thriving infants are more likely to mature faster, to better outcomes and reduced costs.
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: No heat, overheat alarm.
Root cause: Element or thermal fuse failure.
Symptoms: Setpoint error, alarm.
Root cause: Sensor aging.
Symptoms: Uneven warming, hotspot.
Root cause: Blower wear.
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.
Common R&R.
Consumable per patient.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Heating element / thermal fuse Common R&R. | Periodic replacement | $$$ | Moderate |
| Blower fan | Periodic replacement | $$ | Fairly easy |
| Temperature probe Consumable per patient. | Periodic replacement | $ | Easy |
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.
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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