BEUDAMED
    4 results · 28ms · 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 FDA Adverse Event ×

    COBAS 8000 C702 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·October 6, 2025

    HEARTSTART XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 22, 2014

    POWER PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code FPO·October 8, 2010

    VISTA-S ANGELED DEVICE 14X14, 5MM (RED)

    FDA Adverse Event
    Injury ·ZIMMER TRABECULAR METAL TECHNOLOGY·Product code JWH·December 5, 2012