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

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    SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG

    FDA 510(k)
    FDA Class 1 ·General Hospital

    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·05051471150768·K-WIRE - SINGLE TROCAR 1.6mm DIA x 230mm

    QFLOW 500 TITANIUM BOLT, QUAD LUMEN BOLT KIT

    FDA 510(k)
    FDA Class 2 ·Neurology

    SELF RETAINING BICANALICULUS INTUBATION SET

    FDA 510(k)
    FDA Unclassified ·Unknown

    LINOX SD 65/16

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code LWS·December 22, 2010

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·February 4, 2013

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·July 17, 2014