BEUDAMED
    7 results · 48ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Malfunction ×

    HUMIDAIR STANDARD TUBE

    FDA Adverse Event
    Malfunction ·RESMED CORP.·Product code BZD·October 9, 2025

    S8

    FDA Adverse Event
    Malfunction ·RESMED CORPORATION·Product code BZD·March 30, 2010

    RESMED S9 AUTOSET

    FDA Adverse Event
    Malfunction ·RESMED CORPORATION·Product code BZD·October 28, 2016

    RESMED AIRSENSE 10 - AUTOSET

    FDA Adverse Event
    Malfunction ·RESMED CORPORATION·Product code BZD·January 5, 2024

    LIFECHOICE

    FDA Adverse Event
    Malfunction ·INOVA LABS, INC.·Product code CAW·December 16, 2016

    AURA 40 REUSABLE

    FDA Adverse Event
    Malfunction ·BESMED HEALTH BUSINESS CORPORATION·Product code CAE·July 9, 2021

    AMBU AURASTRAIGHT SILICONE

    FDA Adverse Event
    Malfunction ·BESMED HEALTH BUSINESS CORPORATION·Product code CAE·November 13, 2019