BEUDAMED
    2,681 results · 27ms · Sources: EU EUDAMED, US FDA

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    DTF-1000LL,DTF-1000

    FDA 510(k)
    FDA Class 1 ·Dental

    DT Fluid

    FDA UDI
    TCOAG IRELAND LIMITED·15391521421729·

    Trigger-Flex®

    FDA UDI
    ELLIQUENCE, LLC·00846338000288·

    Trigger-Flex®

    FDA UDI
    ELLIQUENCE, LLC·00846338001216·A2E 38cm

    Trigger-Flex®

    FDA UDI
    ELLIQUENCE, LLC·00846338000943·

    Trigger-Flex®

    FDA UDI
    ELLIQUENCE, LLC·00846338000066·S 36cm

    Trigger-Flex®

    FDA UDI
    ELLIQUENCE, LLC·00846338010706·

    Trigger-Flex®

    FDA UDI
    ELLIQUENCE, LLC·00846338000844·M 35cm

    Trigger-Flex®

    FDA UDI
    ELLIQUENCE, LLC·00846338000998·

    Trigger-Flex®

    FDA UDI
    ELLIQUENCE, LLC·00846338000837·

    Trigger-Flex®

    FDA UDI
    ELLIQUENCE, LLC·00846338000936·

    Trigger-Flex®

    FDA UDI
    ELLIQUENCE, LLC·00846338001018·

    Trigger-Flex®

    FDA UDI
    ELLIQUENCE, LLC·00846338000851·

    Trigger-Flex®

    FDA UDI
    ELLIQUENCE, LLC·00846338010713·

    COBE CENTRYSYSTEM 3

    FDA Adverse Event
    Malfunction ·GAMBRO HEALTHCARE·Product code FII·December 20, 1997

    COBE CENTRYSYSTEM 3

    FDA Adverse Event
    Malfunction ·GAMBRO HEALTHCARE·Product code FII·March 14, 1998

    OPTISURE ACTIVE FIXATION, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NVY·March 9, 2017

    COBE CENTRYSYSTEM 3

    FDA Adverse Event
    Malfunction ·GAMBRO HEALTHCARE·Product code FII·October 11, 1996

    COBE CENTRYSYSTEM 3

    FDA Adverse Event
    Malfunction ·GAMBRO HEALTHCARE·Product code FII·December 20, 1997

    COBE CENTRYSYSTEM 3

    FDA Adverse Event
    Malfunction ·GAMBRO HEALTHCARE·Product code FII·October 11, 1996