BEUDAMED
    6 results · 21ms · 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 ×

    REVERSE SHOULDER SYSTEM LAT. GLENOSPHERE 36XØ24.5

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSD·February 7, 2022

    COBAS® WNV NUCLEIC ACID TEST FOR USE ON THE COBAS® 6800/8800 SYSTEMS

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code QHO·September 29, 2025

    OMNIPOD 5 AUTOMATED INSULIN DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code QFG·May 7, 2026

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 7, 2011

    I-PORT

    FDA Adverse Event
    Injury ·PATTON MEDICAL DEVICES·Product code FOZ·February 6, 2008

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO·Product code DTB·February 25, 2008