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

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    Filters Regulation: Us FDA ×

    POROUS MEDIA DBF23 REUSABLE RESPIRATORY FILTER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Nexxis OR

    FDA UDI
    Barco NV·05415334002388·NEXXIS SYSTEM X670 CM

    SERA-TEK THYROGLOBULIN ANTIBODY TEST

    FDA 510(k)
    FDA Class 2 ·Immunology

    SLIDEX STREPTO-KIT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024158696·

    XMAX MOTOR

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code ERL·March 31, 2015

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·February 15, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011

    SYNERGY

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code LGW·July 29, 2014

    MENTOR MEMORYGEL BOOST BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·July 9, 2024