BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    MODULAR ACETABULAR CUP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AST/SGOT Liqui-UV®

    FDA UDI
    STANBIO LABORATORY, L.P.·00657498000496·For the Kinetic Quantitative Determination of A...

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110997·DOUBLE PLASTIC STERILIZATION CASE

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110980·STERILIZING CASE PLASTIC LARGE

    DEWIN

    FDA UDI
    DonneVie Medical Technology(Shanghai)Co.Ltd·16972962310217·Micromanipulation pipette is a disposable steri...

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 8, 2006

    MICROLIFE WRIST WATCH BLOOD PREEURE MONITOR, BP3MO1-3P

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DIATEK CONNECTOR ASSEMBLY REPLACEMENT KIT (CARK)

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

    B1005, ACUCISE ENDOPYELOTOMY SYSTEM

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code EYB·April 17, 2017

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·January 17, 2013

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·AV-REDWOOD CITY·Product code MGB·December 10, 2010

    INTEGRITY ADX DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·July 8, 2014