BEUDAMED
    8 results · 27ms · 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 ×

    VITALOGRAPH-EC60 HYDROGEN MONITOR

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668109373·DVALI CAPSULE POLISHER DUAL PORTS

    RULER

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

    SLT 220 WASHER FOR MICROITITERPLATES

    FDA 510(k)
    FDA Class 2 ·Microbiology

    LOGIC CR TIB INSERT STD, SZ 4, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·November 2, 2022

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 16, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 19, 2010

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 16, 2012