BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    AxoGen Nerve Cap

    FDA 510(k)
    FDA Class 2 ·Neurology

    BIO-CLAD ALL POLY CUP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304255760·

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613054618·Salz Nucleus Splitter, Titanium, Short Colibri ...

    VIGNET TELEHEALTH MANAGER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CATHETER REPAIR KIT WITH REPLACEMENT CONNECTOR, MODEL 5587000

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PRECISION? MONTAGE? MRI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·June 12, 2025

    ANSPACH® MULTA

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code ERL·October 10, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·June 11, 2013

    34 IN SINGLE PORT/SINGLE BLADDER DISPOSABLE

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code KCY·June 22, 2011