BEUDAMED
    6 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.

    SURGITEK ENDOTRACHEAL TUBE, LASER RESIS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CRYOCARE SURGICAL SYSTEM, MODEL CRYO 20

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

    POWDER FREE LATEX PATIENT EXAMINATION GLOVES, WITH PROTEIN CONTENT LABELING CLAIM, NATURAL COLOR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    THERMOPHORE AUTOMATIC HEAT PACK

    FDA Adverse Event
    Malfunction ·BATTLE CREEK EQUIPMENT·Product code IRT·May 2, 2014

    HEMOCHRON SIGNATURE ELITE

    FDA Adverse Event
    Injury ·INTERNATIONAL TECHNIDYNE CORP·Product code DSQ·September 1, 2010

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 2, 2010