BEUDAMED
    9 results · 26ms · 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.

    AT HOME DRUG TEST, MODEL 9175

    FDA 510(k)
    FDA Unclassified ·Unknown

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024157064·

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024157057·

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024157040·

    MERCURY VCO2

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NCB Plating System Distal Femur and Proximal Tibia

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ASAHI APS DIALYZERS

    FDA Adverse Event
    Injury ·ASAHI KASEI MEDICAL CO., LTD.·Product code KDI·March 1, 2013

    PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·February 15, 2011

    ATTAIN ABILITY

    FDA Adverse Event
    Injury ·MPRI·Product code OJX·August 8, 2014