BEUDAMED
    9 results · 18ms · 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.

    CELLTRAK-B

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Zavation

    FDA UDI
    Zavation LLC·00842166194038·Modular Screw 4.5 x 85

    Zavation

    FDA UDI
    Zavation LLC·00842166192775·Modular Screw 4.5 x 85

    ANVIL RETRACTOR

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

    ALBUMIN REAGENT (BCG

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    HS III PROXIMAL SEAL SYS 3.8MM

    FDA Adverse Event
    Injury ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·May 2, 2014

    DURATA STS OPTIM ACTIVE FIXATION LEAD, DF-4 CONNECTO

    FDA Adverse Event
    Death ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·November 15, 2012

    TERUMO STERNAL SAW II

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code GFA·September 9, 2010

    OSTYCUT BONE BIOPSY NEEDLE

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code DWO·September 7, 2015