BEUDAMED
    6 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 ×

    HARDY DISK AMPICILLIN/SULBACTAM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    LASERSAT CO2

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

    RETRIEVAL DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BURR ATTACHMENT ANGLED

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWE·February 27, 2013

    SET,CLEARLINK CONTINU-FLO 3YLL 106 IN 10DPM 48 EA/CA

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SHERBROOKE·Product code FPA·February 16, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014