BEUDAMED
    9 results · 19ms · 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 ×

    MEPIFORM ADHERENT SILICONE DRESSING FOR SCAR CARE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    LPI MULILASE YAG/532 SURGICAL LASER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    AUDIOMETRIC IMPEDANCE TESTER, MODEL Z02020

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    1.5MM RESORB ORBITAL FLOOR PL 24MMX24MM W/BENDING TEMP-STER

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JEY·November 2, 2012

    EMS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·August 12, 1997

    MED, RIGHT, 16 POST AUG UHMWPE GLENOID

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWS·December 19, 2024

    CAREASSIST BED

    FDA Adverse Event
    Malfunction ·HILL-ROM PLUVIGNER·Product code FNL·January 28, 2013

    PARADIGM INSULIN INFUSION PUMP MMT-515LNAB

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·January 21, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 1, 2014