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

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    FEMORAL CEMENT RESTRICTOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NBAC 3.0T SMS, Flex

    FDA UDI
    LMT Medical Systems GmbH·04260486610216·No description.

    Sphero Attachments

    FDA UDI
    Preat Corporation·00842092110805·Sphero Reconstruction Kit 2.2mm Ø

    Convaid

    FDA UDI
    CONVAID PRODUCTS, INC.·00840117408494·

    THD PressProbe

    FDA UDI
    THD SPA·08033737711286·THD PressProbe is a disposable active probe for...

    Convaid

    FDA UDI
    CONVAID PRODUCTS, INC.·10840117400877·

    n/a

    FDA UDI
    Ortho Development Corporation·00822409104505·Troch Nail, Ball Locking Hex Driver, Nail

    0800,APS1,08,N,VL,JW

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828152877·0800,APS1,08,N,VL,JW

    MANDREL GUIDEWIRES OR M-WIRES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NIPRO INSULIN SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HWC·May 8, 2014

    ACCU-CHEK SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·October 17, 2012

    PLUM XLM W/MODIFD B

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·August 10, 2010

    VIDAS® HCG 60 TESTS

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code JHI·February 9, 2022