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

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    ACUPUNCTURE NEEDLES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ZEUS-P

    FDA UDI
    SPINAL ELEMENTS, INC.·00840606160834·FLAT PADDLE DISTRACTOR, 6MM

    YELLOW SPECIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    SURGICAL MEDICAL DEVICE CAUTERY

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    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

    IBP ELB INT. ULNA LRG RGT LNG STM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·June 24, 2016

    HAMMER 500 GRAMS

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code FZY·April 9, 2013

    ISERT ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·HOYA SURGICAL OPTICS INC.·Product code HQL·February 25, 2011

    EASYTRAK 3

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code DTB·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

    BD VACUTAINER® K2 EDTA (K2E) PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·September 25, 2018

    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