BEUDAMED
    15 results · 26ms · Sources: EU EUDAMED, US FDA

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    Braun Silk.expert Mini

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

    ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101

    FDA 510(k)
    FDA Unclassified ·Unknown

    SMITH & NEPHEW CANNULATED SCREWS AND WASHERS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GENESIS

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC., ORTHOPAEDICS DIV.·Product code HSH·February 3, 1999

    TSRH SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·SOFAMOR DANEK MFG·Product code KWP·May 29, 1998

    CRYOVALVE

    FDA Adverse Event
    Injury ·CRYOLIFE, INC.·Product code MIE·October 9, 1998

    C.D. SCREWS AND RODS

    FDA Adverse Event
    Injury ·SOFAMOR DANEK·Product code MCV·October 26, 1994

    ENDOPATH

    FDA Adverse Event
    ETHICON·July 29, 1994

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·July 8, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 29, 2014

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 8, 2013

    PERCUFLEX 6 FR X 26CMS DJ STENT

    FDA Adverse Event
    Injury ·MICROVASIVE·Product code MER·August 29, 1994

    REDUCTION FORCEPS WITH SERRATED JAW-RATCHET 144MM

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTD·March 20, 2019

    ZIMMER SKIN GRAFT MESHER

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code FZW·November 1, 2013

    OMNIGUIDE 4F GUIDING CATHETER

    FDA Adverse Event
    Other ·MEDTRONIC MIS·Product code DQO·May 11, 1998