BEUDAMED
    10 results · 30ms · Sources: EU EUDAMED, US FDA

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    ELECATH BALTHERM TLC THERMAL DILUTION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GE DATEX-OHMEDA AVANCE CS2

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ARTHREX TRIMIT SCREW, MODEL AR-4161B

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ENDOWRIST ONE VESSEL SEALER

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL INC.·Product code NAY·May 20, 2014

    FLEXIMA¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code FFA·November 14, 2012

    NEURON DELIVERY CATHETER 070

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DQY·September 7, 2010

    S-ROM*SLEEVE PRX ZTT, 18D-LRG

    FDA Adverse Event
    Injury ·DEPUY (IRELAND) - 9616671·Product code LPH·July 27, 2015

    S-ROM*SLEEVE PRX ZTT, 18D-LRG

    FDA Adverse Event
    Injury ·DEPUY (IRELAND) - 9616671·Product code LPH·July 27, 2015

    ASR TAP SLV ADAP 11/13 +0

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 27, 2015

    SROM STM STD 36+12L 13X18

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code MRA·July 27, 2015