BEUDAMED
    22 results · 29ms · Sources: EU EUDAMED, US FDA

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    FDA 510(k)
    FDA Class 2 ·Radiology

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486001209·MCK Inlay Tibial Component

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486001858·MCK Inlay Tibial Component

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486001896·MCK Inlay Tibial Component

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486001865·MCK Inlay Tibial Component

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486001889·MCK Inlay Tibial Component

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486001193·MCK Inlay Tibial Component

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486001841·MCK Inlay Tibial Component

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486001186·MCK Inlay Tibial Component

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486001872·MCK Inlay Tibial Component

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197086059·DESCHAMPS Ligature needle 21.0 c...

    SignaLoc Screw

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215116750·

    HYLATOPICPLUS CREAM

    FDA 510(k)
    FDA Unclassified ·Unknown

    LIQUID ASSAYED MULTIQUAL 1, LIQUID ASSAYED MULTIQUAL 2, LIQUID ASSAYED MULTIQUAL 3, LIQUID ASSAYED MULTIQUAL MINIPAK

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CUP: MPACT ACETABULAR SHELL Ø52 MULTI-HOLE

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·November 26, 2019

    VERSACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·September 8, 2014

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·August 27, 2018

    ACTIVA

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code MHY·June 20, 2013

    CESAR-OMCP-VISUB (HM3000)

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code IZF·May 5, 2011

    MODEL S6 ELECTRIC DERMATOME SET, COMPLETE

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code GFD·October 15, 2014