BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    AURAFLEX CK-MB 200TEST PACK, CALIBRATOR PACK

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Brigade

    FDA UDI
    Nuvasive, Inc.·00887517400703·Brigade Implant, 16x38x28mm 12°

    Brigade

    FDA UDI
    Nuvasive, Inc.·00887517195081·Brigade Trial, 16x38x32mm 12°

    MEDTRONIC EXTENDED

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 26, 2024

    INVERNESS MEDICAL TESTPACK + PLUS STREP A WITH OBC

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Phenom 17 Catheter, Phenom 21 Catheter, Phenom 27 Catheter, Phenom Plus Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·February 9, 2013

    CORE IMPACTION DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code DZJ·July 23, 2014

    FLEXTEND

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·January 6, 2011

    MEDTRONIC EXTENDED

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 26, 2024