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AB ULAX

SE Last updated 23 Oct 2026

Devices
0
Registries
FDA
FDA recalls
1

Catalogue0

No devices listed yet from this manufacturer.

FDA recalls1

Recalls this firm reported to the FDA. Device pages show the recalls that name the device or the 510(k)/PMA it was cleared under.

  • 2020

    • 4 Sep 2020 Z-0059-2021 Class II Terminated Firm has received 6 complaints that the Heat Moisture Exchanger (HME) disconnected from the closed respiratory circuit during use. If the HME separates, the ventilator circuit may not provide adequate ventilation to the patient, potentially resulting in lack of oxygen leading to hypoxia or death.

Information

Country
SE
Address
MERKURIUSGATAN 8, MOTALA Ostergotland
FDA FEI number
3004030908