BEUDAMED
    7 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.

    OPIATES MICRO-PLATE ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Regatta Lateral System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981090999·Kerrison Punch, 5mm

    IMMOBILE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LATERAL BUTTRESS SUPPORT

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

    840 VENTILATOR

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·June 23, 2014

    ASR ACETABULAR CUPS 60

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 30, 2013

    CRE(TM) BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KOG·December 22, 2010