BEUDAMED
    6 results · 24ms · 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 ×

    SELECT(R) SHOULDER ALL-POLY GLENOID

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DIGITAL FLAT PANEL X-RAY DETECTOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    PRO-PACT PERACETIC ACID CULTURE TEST KIT, MODEL C-3PA

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RSP SHOULDER

    FDA Adverse Event
    Malfunction ·ENCORE MEDICAL, L.P.·Product code LXH·November 11, 2010

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·January 28, 2013

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE REHABILITATION EQUIP·Product code FSA·July 14, 2014