BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

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    DOWD(TM) II

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

    BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·TRI-TECH FORENSICS, INC.·Product code JKA·July 29, 2025

    BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·TRI-TECH FORENSICS, INC.·Product code JKA·July 29, 2025

    BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·TRI-TECH FORENSICS, INC.·Product code JKA·July 29, 2025

    JR MEDIC Nitrile Examination Gloves Powder Free (Orange, Purple)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ARMSTRONG V TUBE SUCTION INSERTER

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    LOCKING SCREW, FULLY THREADED 5X35 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·December 8, 2011

    JUVEDERM ULTRA XC 1 ML ROW

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LMH·January 11, 2013

    CONCERTO CRT-D DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·December 13, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 5, 2014