BEUDAMED
    12 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    5000Z FIREFLY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    Starbond CoS

    FDA UDI
    S & S Scheftner GmbH·04260207850372·Disc basic, 18 mm ø 99,5 mm / without edging

    HHM

    FDA UDI
    Oticon A/S·05707131261908·H100, BTE 13 WL 100 DBL HHM

    N/A

    FDA UDI
    TETRA MEDICAL SUPPLY CORP.·00614138105669·NEOPRENE WRAP-AROUND KNEE, REG

    ELATION® MB

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K133552621·ELATION® MB Base Rx 022 UL/5-5 CS-BC HK

    K133532

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·February 2, 2021

    CELLSEARCH CIRCULATING TUMOR CELL KIT MODEL 7900001

    FDA 510(k)
    FDA Class 2 ·Immunology

    LIGHTSPEED 6.0 CT SCANNER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    LAG SCREWDRIVER 380X110MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HXX·May 13, 2010

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·May 29, 2013

    INLAY OPTIMA URETERAL STENT

    FDA Adverse Event
    Injury ·C.R. BARD, INC.·Product code FAD·June 15, 2011

    EXTRACTOR XL TRIPLE LUMEN RETRIEVAL BALLOON

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GCA·August 22, 2008