BEUDAMED
    8 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 ×

    SILVERLON ISLAND WOUND DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    Bathtub

    FDA UDI
    Ropox A/S·05707581004131·

    ACCUSCULPT II LASER SYSTEM

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

    NANMA VACUUM PUMP PROXZEK MODEL 2M9498S

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    IVT DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MALTA·Product code KPE·October 4, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    COATED VICRYL (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    ETHICON, INC.·Product code GAM·June 17, 2011

    OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021