BEUDAMED
    8 results · 24ms · 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 ×

    ONE COAT BOND DENTIN/ENAMEL ADHESIVE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668109403·SHAPIRO CAPSULE POLISHER CURVED

    SHAPIRO CAPAULE POLISHER

    FDA Adverse Event
    Injury ·KATENA PRODUCTS INC.·Product code HMX·December 28, 2022

    AUTO EIA MICROPLATE READ MODEL CERES 900 W/VAR OPT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SHARPOINT POLYPROPYLENE NONABSORB SURG SUTURES USP

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

    HEARTSTART MRX -EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 11, 2014

    SMALL BATTERY DRIVE

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HWE·February 22, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC.·Product code NBW·January 31, 2011