BEUDAMED
    24 results · 21ms · Sources: EU EUDAMED, US FDA

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    WOOJEON ACUPUNCTURE NEEDLE (=SERA ACUPUNCTURE NEEDLE)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NA

    FDA UDI
    Smith & Nephew, Inc.·00885556007716·BONE CURETTE CURVED 45 DEG 228.6 ...

    Bernafon

    FDA UDI
    Bernafon AG·05711584004449·CT5 CP, VC PS BE CANTEO 5

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450299562·

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776164683·HEANEY RETR . LARGE

    Depth gauge

    FDA UDI
    Jeil Medical Corporation·08800089431106·

    Summa Orthopaedics System Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08800089466412·

    MICRA LENS INJECTOR, MICRA CARTRIDGE LENS, MICRA LENS LOADER

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    NEOPAC SOFTWARE, 3007 DIGITAL PHOTOMETER/FLUOROMETER MODEL NA, 307 AND 350D

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    NV GXL LINER NEUTRAL, 32MM ID GROUP 1 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·September 5, 2024

    NV GXL LINER LIPPED 32MM ID, GROUP 1 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·September 5, 2024

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 13, 2024

    ALT HA S CLR EXT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code MEH·November 14, 2023

    ASR ACETABULAR IMPLANT 62

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·May 14, 2013

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·September 23, 2014

    ASR UNI FEMORAL IMPL SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·May 13, 2011

    NV GXL LINER NEUTRAL, 36MM ID, GROUP 2 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·May 31, 2024

    NV GXL LINER NEUTRAL, 32MM ID GROUP 1 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·August 12, 2024

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·February 3, 2015

    BIOLOX DELTA FEMORAL HEAD 32MM OD, -3.5MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·October 3, 2024