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

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    FIXATION WIRE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·00636257073391·PROTECT PATELLA TRACKING BRACE, RT, 2X

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909115052·REVELATION DIAMOND SE6-016F - 5 PACK

    Novo Surgical

    FDA UDI
    NOVO SURGICAL, INC.·G5869115050·round caps, gas or steam permeable, can be used...

    "1.5MM" SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036053260·

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756020558·FINGER SPLINTS

    RTVUE CAM WITH CORNEAL POWER UPGRADE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    IMMULITE INTACT PTH, MODEL LKPP1 (100 TESTS), LKPP5 (500 TESTS), IMMULITE 2000 INTACT PTH, MODEL L2KPP (200 TESTS), L2K6

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    REZUM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·October 6, 2025

    REZUM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·October 6, 2025

    REZUM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·January 7, 2026

    REZUM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025

    REZUM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·March 13, 2026

    REZUM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025

    REZUM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025

    SYNCHRON® ALT REAGENT, 2 X 200 TEST

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code CKA·July 26, 2011

    REZUM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·January 13, 2026

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·January 11, 2013

    CAROTID WALLSTENT MONORAIL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIM·December 1, 2010

    32MM +8 LFIT V40 HEAD

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·July 3, 2014