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 ×

    SCOTTS SURGICAL RETRACTOR AND ELASTIC

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

    OXYGEN CONCENTRATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TUBE, LEATHERMAN/IMBRUCE

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

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 6, 2014

    SENSIA SR

    FDA Adverse Event
    Death ·MEDTRONIC MED REL, INC.·Product code NVZ·October 15, 2012

    WARM AIR

    FDA Adverse Event
    Malfunction ·CINCINNATI SUB-ZERO PRODUCTS, INC.·Product code DWJ·August 4, 2010