BEUDAMED
    39 results · 24ms · Sources: EU EUDAMED, US FDA

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    ADVANIX DOUBLE PIGTAIL BILIARY STENT

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Molar Rotation2 Appliance

    FDA UDI
    Ortho Organizers, Inc.·00190707064488·NITANIUM® MOLAR ROTATOR2 APPLIANCE (36mm)

    VACUETTE SAFETY BLOOD COLLECTION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TEMPORARY GINGIVAL CUFF AND IMPRESSION POST AND IMPLANT ANALOG

    FDA 510(k)
    FDA Class 2 ·Dental

    TAPERLC BMPC LAT 6.0X132 12/14

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code KWA·August 4, 2016

    TAPERLOC PC 15.0 MM 12/14

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code KWA·August 4, 2016

    EVOKE CLOSED LOOP STIMULATOR (CLS)

    FDA Adverse Event
    Injury ·SALUDA MEDICAL PTY LTD·Product code LGW·April 28, 2025

    2520274-2013-02472

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·May 9, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 10, 2011

    LIGACLIP ALLPORT ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC·Product code OCW·August 5, 2008

    TAPERLOC COMPLETE MICROPLASTY FEMORAL

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 20, 2017

    TPRLC 133 TYPE1 BM SO 11.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·September 12, 2018

    TAPERLOC BONEMASTER POROUS AND HYDROXYAPETITE COATED STEM

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code KWA·May 26, 2017

    TAPERLOC TYPE1 BM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·December 4, 2018

    TPRLC 133 FP TYPE1 BM HO 10.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 13, 2018

    TPRLC 133 MP TYPE1 BM HO 10.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 20, 2019

    TAPERLOC STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 19, 2017

    TAPERLOC FEMORAL STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·December 22, 2016

    TAPERLOC COMPLETE PRIMARY FEMORAL POROUS-BONEMASTER REDUCED DISTAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 6, 2018

    COREVALVE TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·April 1, 2024