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 ×

    3B RESMART BPAP 25A, BMC RESMART BPAP 25A

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    GPSCATH BALLON DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EIUS UNICOMPARTMENTAL KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 29, 2025

    ACCUSOL

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CASTLEBAR·Product code KPO·June 20, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

    ADVIA CENTAUR CP

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code MMI·October 1, 2014