BEUDAMED
    51 results · 20ms · Sources: EU EUDAMED, US FDA

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    SCARLET AC-T SECURED ANTERIOR CERVICAL CAGE AND ASSOCIATED INSTRUMENTATION

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Biomet® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00887868558825·

    Covid 19 Testing Kit

    FDA UDI
    Ditek Consulting, LLC·00860011770268·Covid 19 Testing Kit

    BIOMET KNEE SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304006706·

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221037237·Unitek(TM) Bicuspid Band General Purpose Wide U...

    SCHWERT

    FDA UDI
    A. Schweickhardt GmbH & Co. KG·E8961413140·Periosteal elevators 11mm

    K2M General Instruments

    FDA UDI
    VB Spine LLC·10888857580893·Split Tube Retractor Ø20x60 mm

    Responsive Orthopedics Total Knee Arthroplasty System

    FDA UDI
    RESPONSIVE ORTHOPEDICS, LLC·00841973101642·Poly Insert MPCS, Size 3R, 14mm

    ADVANIX BILIARY STENT WITH NAVIFLEX RX DELIVERY SYSTEM

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

    MORPHEUS OX

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·April 20, 2026

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 1, 2026

    ADVANIX BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·January 8, 2025

    BD POSIFLUSH

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026

    BD POSIFLUSH

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026

    BD POSIFLUSH NORMAL SALINE SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·January 6, 2021

    ADVANIX BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 5, 2024

    SYRINGE 10ML REG PR SALINE 10ML FILL

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code NGT·August 5, 2021

    SPRINT FIDELIS

    FDA Adverse Event
    Death ·MPRI·Product code LWS·June 3, 2013

    X8000 LIGHTSOURCE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY SAN JOSE·Product code FCW·June 1, 2011