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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    IMMULITE (TM) TOTAL T3

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ComposiTCP

    FDA UDI
    S.B.M·03760154007191·Absorbable interference screw

    3M™ Victory Series™

    FDA UDI
    3M UNITEK CORPORATION·00652221113214·3M™ Victory Series™ Second Molar Bands, 905-214...

    BIOPSY NEEDLE TRANSPONDER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    RIGID URETEROSCOPE

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

    BD PLASTIPAK LUER-LOK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·August 9, 2019

    TANDEM T:SLIM INSULIN DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE INC.·Product code LZG·May 29, 2014

    QUICKFLEX MICRO LV LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·January 9, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 22, 2010