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

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    SLED UNICOMPARTMENT KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471183797·K-WIRE - SINGLE TROCAR 1.8mm DIA x 150mm

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123175·K-WIRE - SINGLE TROCAR THREADED 1.8mm DIA x 150mm

    IN VITRO TEST DETERMINATION OF SGPT(ALT)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Azurion R3.1

    FDA 510(k)
    FDA Class 2 ·Radiology

    DEPUY ASR XL FEM IMP SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 11, 2013

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 10, 2011

    ASR ACETABULAR CUPS 54

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 23, 2014

    ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS. For neurological endovascular use.

    FDA Enforcement
    Class I ·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020