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

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    2.3MP Color LCD Monitor, RadiForce MX242W

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526550216·GENUMEDI PT KNEE SUP SILVER R EW VI

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814176·GENUMEDI PT SILVER R I

    AUVON RECHARGEABLE TENS UNIT MUSCLE STIMULATOR

    FDA Adverse Event
    Injury ·SHENZHEN AS-TEC TECHNOLOGY CO., LTD·Product code NGX·January 27, 2025

    HARVEST GRAFT DELIVERY SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    EUROIMMUN ANTI-NRNP/SM ELISA (IGG)

    FDA 510(k)
    FDA Class 2 ·Immunology

    CONFIRM

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC. CRMD·Product code MXC·January 13, 2014

    ACCU-CHEK ® COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 3, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·June 28, 2011

    AUVON TENS UNIT

    FDA Adverse Event
    Injury ·SHEN ZHEN AS TEC TECHNOLOGY CO LTD·Product code NUH·December 19, 2024

    1823260-2017-00646

    FDA Adverse Event
    Malfunction ·March 27, 2017

    COBAS E 411 IMMUNOASSAY ANALYZER

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·February 21, 2017