BEUDAMED
    8 results · 34ms · 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.

    MALT AGAR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    NA

    FDA UDI
    Richard Wolf GmbH·04055207010280·OP-MICROLARYNGOSCOPE WL 103MM outer dimension ...

    VAPOR-PHASE HUMIDIFIER SYS-ADVANCED

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MUSE-DP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FAN SPRAY KIT

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code FQH·February 28, 2023

    EXOSEAL VASCULAR CLOSURE DEVICE (VCD)

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code MGB·June 3, 2014

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 26, 2012

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·September 27, 2010