BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

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    DEGUFILL (R) BOND

    FDA 510(k)
    FDA Class 2 ·Dental

    MILLENNIUM 9000 PHASED ARRAY NEUROVASCULAR COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    TORNIER, PITON FIXATION IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GMK-SPHERE PATELLA RESURFACING SIZE 2

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·March 25, 2021

    ACCU-CHEK ® AVIVA COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·June 30, 2014

    MAXI PTA BALLOON CATHETER

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code LIT·November 17, 2010

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·November 21, 2012

    SMR REVERSE HUMERAL BODY

    FDA Adverse Event
    Injury ·LIMACORPORATE SPA·Product code KWS·November 23, 2020

    1.5 LACTOSORB SYSTEM 1.5 X 5 MM LACTOSORB SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·August 22, 2018

    5.0MM LOCKING SCREW SLF-TPNG WITH T25 STARDRIVE RECESS 36MM

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code KTT·October 10, 2018