FDA Device Intelligence
HomeIMT Analytics AG › EVair

EVair

IMT Analytics AG · Model M1230847 · UDI-DI 76402146418924

BTI Prescription
10
510(k) clearances
5,408
Adverse events (36 deaths)
5
Recalls
72
Facilities

Description

The medical air compressor is intended for use as an integrated, optional accessory to provide a dry, filtered, breathable compressed air supply to GE Datex-Ohmeda Engström Carestation and Engström Pro ventilators.

Recalls

DateFirmReason
2023-12-29Datex-Ohmeda, Inc.GE HealthCare has become aware of elevated levels of formaldehyde when the EVair or EVair 03 (Jun-Air) optional compressors are used with the CARESCAPE R860 or Engstrm Carestation/
2023-12-29Datex-Ohmeda, Inc.GE HealthCare has become aware of elevated levels of formaldehyde when the EVair or EVair 03 (Jun-Air) optional compressors are used with the CARESCAPE R860 or Engstrm Carestation/
2023-12-29Datex-Ohmeda, Inc.GE HealthCare has become aware of elevated levels of formaldehyde when the EVair or EVair 03 (Jun-Air) optional compressors are used with the CARESCAPE R860 or Engstrm Carestation/
2013-12-05Maquet Cardiovascular Us Sales, LlcMaquet Compressor Mini may deliver compressed air at a temperature higher than specified.
2007-01-26Draeger Medical, Inc.Compressors not providing sufficient supply pressure to connected medical ventilator

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.