BEUDAMED
    11 results · 27ms · Sources: EU EUDAMED, US FDA

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    VITAACCESS CATHETER INTRODUCER KIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    INTERSEPT* BLOOD FILTER W/ TUBING BYPASS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VERTECEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VERTECEM V+ CEMENT KIT

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code NDN·March 28, 2013

    VERTECEM V+ CEMENT KIT

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code NDN·February 27, 2013

    VERTECEM V+ CEMENT KIT

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code NDN·March 1, 2013

    VERTECEM V+ CEMENT KIT

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code NDN·February 27, 2013

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code MMI·December 30, 2012

    HEAD RIGHT TIMING LINK ASSY

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code FNL·October 27, 2010

    UNIFY CRT-D, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D·Product code NIK·January 13, 2014

    TRULIANT TIB IMP PS INSERT SZ 3.5 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·January 24, 2023