BEUDAMED
    7 results · 26ms · 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.

    WIRE TWISTERS

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

    QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLE

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

    ATEC Lateral Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NEURON DELIVERY CATHETER 053

    FDA Adverse Event
    Malfunction ·PENUMBRA INC.·Product code DQY·March 15, 2010

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·May 6, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 13, 2012

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015