BEUDAMED
    7 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.

    COBAS-BIO CENTRIFUGAL ANALYZER

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    VERTEBRIS

    FDA UDI
    Richard Wolf GmbH·04055207020784·PUNCH Ø 2.6MM WL 360MM color code orange, TL 4...

    Hemostatic Xerogel Sponge

    FDA 510(k)
    FDA Unclassified ·Unknown

    VARIAX ELBOW SYSTEM LINE EXTENSION

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code LJH·May 6, 2014

    OT VERIO IQ METER

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

    THERA-I DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·August 11, 2010