BEUDAMED
    58 results · 23ms · Sources: EU EUDAMED, US FDA

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    DIMENSION VISTA A1AT FLEX REAGENT CARTRIDGE AND PROTEIN 1 CALIBRATOR AND CONTROL MEDIUM AND HIGH

    FDA 510(k)
    FDA Class 2 ·Immunology

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

    FDA UDI
    FX SOLUTIONS·03701037312568·36/10 HUMELOCK REVERSED BROACH

    LFIT

    FDA UDI
    Howmedica Osteonics Corp.·07613327072372·Femoral Head

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180500972·Slap Hammer Adapter, 1/4" Sq

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

    FDA UDI
    FX SOLUTIONS·03701037317631·36/10 HUMELOCK REVERSED BROACH WITH RADIUS

    HDL-CHOLESTEROL PLUS 2ND GENERATION

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    PERIFIX SAFETY EPIDURAL NEEDLES

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FLIPPER 110 PDA CLOSURE COIL DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code KRD·January 2, 2017

    MREYE FLIPPER PDA CLOSURE DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code KRD·June 13, 2018

    TRIDENT 10 X 3 INSERT 36MM ID

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code LPH·February 24, 2010

    TRIDENT PSL WITH PUREFIX HA

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·June 24, 2011

    FLIPPER 110 PDA CLOSURE COIL DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code KRD·March 8, 2017

    MREYE FLIPPER PDA CLOSURE DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code KRD·March 8, 2017

    TRIDENT PSL WITH PUREFIX HA

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·June 24, 2011

    TRIDENT PSL WITH PUREFIX HA

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·June 24, 2011

    TRIDENT 0 CROSSFIRE INSERT 36 MM ID

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code LPH·August 13, 2012

    HUDSON ENDOTRACHEAL TUBE, HVT, 7.5

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code BTR·April 12, 2013

    AXSYM RUBELLA IGG ANTIBODY

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code LFX·June 19, 2008

    PK7312-03 AUTOMATED MICROPLATE SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER MISHIMAK.K.·Product code KSZ·April 19, 2011

    MREYE FLIPPER PDA CLOSURE DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code KRD·February 7, 2017