BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    REMEL RIM STREPTOCOCCUS GROUPING LATEX AGGLUTINATION TEST

    FDA 510(k)
    FDA Class 1 ·Microbiology

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150775·K-WIRE - SINGLE TROCAR 2.0mm DIA x 230mm

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123038·K-WIRE - DOUBLE TROCAR 0.9mm DIA x 75mm

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150690·K-WIRE - SINGLE TROCAR 0.9mm DIA x 75mm

    V20 SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    VANGUARD M SERIES UNICONDYLAR TIBIAL BEARINGS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ASR UNI FEMORAL IMPL SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTL, LTD·Product code KWA·December 17, 2010

    IVT DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MALTA·Product code KPE·July 17, 2014

    SETROX S 53

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVZ·December 27, 2012

    DIMENSION EXL 200

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code JJE·July 23, 2013