BEUDAMED
    28 results · 28ms · Sources: EU EUDAMED, US FDA

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    VIAGRAF DBM PASTE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Navagio

    FDA UDI
    Kalitec Direct LLC·B07330K0132090·Trial, TLIF, 27L OB CRV 7Deg, 9mm

    K-WIRE GAMMA Ø3,2X450 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·March 20, 2016

    URINE OPIATES (OPI) SCREEN FLEX REAGENT CARTRIDGE, CATALOG NO. DF93A

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    INSIGHT MILLENNIUM III

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    K-WIRE GAMMA Ø3,2X450 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·March 20, 2016

    UNKNOWN

    FDA Adverse Event
    Malfunction ·COOK, INC.·Product code DTK·August 21, 2014

    UNK

    FDA Adverse Event
    Injury ·COOK, INC.·Product code DTK·August 20, 2014

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·August 20, 2014

    ZOOM

    FDA Adverse Event
    Malfunction ·EXTERNAL MANUFACTURER·Product code KRG·April 9, 2013

    EASYPUMP

    FDA Adverse Event
    Malfunction ·I-FLOW CORPORATION·Product code MEB·February 24, 2011

    CONTAK RENEWAL 4

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code NIK·May 8, 2008

    GUNTHER TULIP VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·April 3, 2026

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·December 5, 2017

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DTK·November 1, 2017

    GUNTHER TULIP VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·November 4, 2025

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·February 27, 2018

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·May 5, 2017

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DTK·May 12, 2017

    UNKNOWN

    FDA Adverse Event
    Injury ·Product code DTK·August 20, 2020