BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    S3 CARDIOPLEGIA CONTROL

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Bioseal Inc.

    FDA UDI
    BIOSEAL·00630094196237·Amber Tubing w/Connector

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111048·INSTRUMENT CASE SMALL ALUMINUM

    SURGISIS PEYRONIE'S REPAIR GRAFT, MODEL SPR-100

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    DIFCO CHLAMYDIA DIRECT DETECTION SYSTEM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·February 14, 2013

    ASR ACETABULAR IMPLANT 58

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code KWA·January 7, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2014