BEUDAMED
    7 results · 20ms · 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 ×

    AMP ALKALINE PHOSPHATASE REAGENT KIT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CORIN MINIHIP STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ICS MEDICAL CHARTR EP WITH ASSR AND CHARTR OAE SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    DWF CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code DWF·December 15, 2016

    NEXGEN FEMORAL PROVISIONAL IMPACTOR/EXTRACT

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·November 30, 2010

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·January 28, 2013

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 14, 2014