BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    PANAVIA SA Cement Universal

    FDA 510(k)
    FDA Class 2 ·Dental

    Percutaneous Compression Plate (PC.C.P)

    FDA UDI
    ORTHOFIX SRL·18032568866117·GOTFRIED PC.C.P. SHAFT SCREW - 37 MM "PACK OF 5"

    Percutaneous Compression Plate (PC.C.P)

    FDA UDI
    ORTHOFIX SRL·18033509850677·GOTFRIED PC.C.P. SHAFT SCREW - 37 MM "PACK OF 5...

    ET III SA ULTRA WIDE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    MODIFICATION TO MEDWAVES MICROWAVE COAGULATION/ABLATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 18, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 11, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 22, 2013

    REVERSE SHOULDER SYSTEM GLENOSPHERE 39XØ24.5

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·May 27, 2020

    REVERSE SHOULDER SYSTEM 04.01.0122 HUMERAL REVERSE HC LINER Ø39/+0MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·November 28, 2022