BEUDAMED
    8 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 ×

    ACE CUSTOM SURGICAL PACK

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

    Speculum, Rectal Kit

    FDA UDI
    CLEARWATER COLON HYDROTHERAPY, INC.·B424922648·Speculum, Rectal Bulb Style Small Speculum Kit ...

    LARGE AO COUPLING ASNIS III HALL FITTING

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·September 25, 2012

    5000 Compact Series Ultrasound Systems (Ultrasound System 5500 G, Ultrasound System 5500 P, Ultrasound System 5500 W, Ultrasound System 5500 CV, Ultrasound System 5300 G, Ultrasound System 5300 P, Ultrasound System 5300 W)

    FDA 510(k)
    FDA Class 2 ·Radiology

    ENDOVIVE INITIAL PLACEMENT DIRECT PEJ KIT, MODELS 6520 & 6521

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

    ASR ACETABULAR IMPLANT 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 18, 2013

    SIGMA 200 D

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code DXY·December 13, 2010

    INTERSTIM

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 9, 2014