BEUDAMED
    56 results · 25ms · Sources: EU EUDAMED, US FDA

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    Volcano iFR Modality, iFR Scout feature

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526768451·GENUMEDI PSS GREEN I

    OSS™ Orthopedic Salvage System

    FDA UDI
    Biomet Orthopedics, LLC·00880304239623·

    HHM

    FDA UDI
    Oticon A/S·05707131288868·H110V2 TI, RITE 312 WL CBE HHM

    Symmetry Surgical Ultra®

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482055519·Ultra Instruments Clamp; Bulldog Artery Clamp; ...

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100127·KRATZ-BARRAQUER SPECULUM RIGHT EYE

    Tibial Regular Trial Insert Size 5

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215073879·

    XINIWAVE, MODEL XW-18

    FDA 510(k)
    FDA Class 2 ·Neurology

    TAPER 2 POROUS FEMORAL STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962110997·BULLDOG ARTERY CLAMP, 1 1/2", STR, TITANIUM

    PRIMORIS HIP STEM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·August 5, 2016

    PRIMORIS FEMORAL STEM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·October 3, 2017

    PRIMORIS NECK PROSTH BM SZ 26

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·August 4, 2016

    PRIMORIS HIP STEM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·August 5, 2016

    PRMRS NCK STEM TI BM SZ 24 RSA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·June 23, 2016

    TAPERLOC LAT COCR 10MM T1

    FDA Adverse Event
    Death ·BIOMET UK LTD.·Product code JDI·March 20, 2026

    TPRLOC COCR CMTD STEM T1 7.5MM

    FDA Adverse Event
    Death ·BIOMET UK LTD.·Product code JDI·March 20, 2026

    UNKNOWN PRIMORIS HIP

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·August 4, 2016

    PRMRS NCK STEM TI BM SZ 24 RSA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWY·April 13, 2018

    GLOVE SURGICAL PROTEXIS PI

    FDA Adverse Event
    Injury ·CARDINAL HEALTH·Product code KGO·June 6, 2013