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

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    NITRILE EXAMINATION GLOVES (WHITE, BLUE AND BLACK)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780165088·Integra® Jarit® Finochietto Needle Holder, 10-1...

    CHS

    FDA UDI
    Smith & Nephew, Inc.·03596010062642·COMPRESSION HIP SCREW SUPER LAG SCREW 115MM

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450639931·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450389980·

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383576482·Gutta Percha Points is used to root canal filin...

    NATURELLE DAILY DISPOSABLE (HILAFILCON B) COSMETICALLY TINTED CONTACT LENS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    QACA IGG/IGM ELISA KIT HRP

    FDA 510(k)
    FDA Class 2 ·Immunology

    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

    CONTOUR

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·April 29, 2014

    ALT HA S CLR EXT

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

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·August 30, 2013

    CONTOUR

    FDA Adverse Event
    Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code NBW·April 5, 2019

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code KWA·June 1, 2011

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    KENSTONE METAL·Product code ITJ·May 20, 2013

    OPTIFLUX 160NR DIALYZER FINISHED ASSEMBLY

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code FJI·July 28, 2014

    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

    BIOLOX DELTA FEMORAL HEAD 32MM OD, -3.5MM

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