BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    PULPDENT ENDODONTIC POST CEMENT KIT

    FDA 510(k)
    FDA Class 2 ·Dental

    X-CORE

    FDA UDI
    Nuvasive, Inc.·00887517270436·XC Mini Endcap, 17x14mm 7° Lord Top Ø12

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295244288·P.F.C. SIGMA TIBIAL INSERT FIXED BEARING STABIL...

    ELITE

    FDA UDI
    DEPUY (IRELAND)·10603295244295·ELITE FEMORAL HEAD +6 9/10 TAPER Diameter 28mm

    Proture Double Electric Breast Pump

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ARTHREX RETROBUTTON, 15MM, 60MM, RETROBUTTON, LONG, 15MM, 60MM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEARTSTART FRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 13, 2014

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    KENSTONE METAL·Product code IKX·February 14, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP MMT-522NAS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·January 11, 2011

    Depuy P.F.C. E Knee System, stabilized plus tibial insert; polyethylene tibial insert, Sz 4, 30 mm; Ref 96-2747.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·May 26, 2005

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·February 6, 2017