BEUDAMED
    7 results · 20ms · 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 Regulation: Us FDA ×

    RELiZORB®

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BD SAFETYGLIDE¿ SAFETY NEEDLE 27 G X 1/2 IN

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code MEG·September 22, 2017

    ILT SAFE-CROSS DEFLECTING CATHETER, MODEL C114ND1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TightRail Guardian Motorized Dilator Sheath

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MONOPOLAR CURVED SCISSORS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC.·Product code GEI·November 14, 2008

    ASR ACETABULAR IMP 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·August 18, 2011

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 18, 2013