BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    RAPID DISCONNECT Y-SET, CAT. NO. 48-7000

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    VPAP III

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SAFESEPT NEEDLE FREE TRANSSEPTAL TROCAR GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 22, 2015

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 28, 2013

    POLYHESIVE PATIENT RETURN ELECTRODE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code GEI·December 16, 2010

    InterGard Knitted Collagen Coated Vascular prostheses marketed under 510(k) # K964625; InterGard Woven Collagen Coated Vascular prostheses marketed under 510(k} #K970843 and K984294.

    FDA Recall
    Terminated ·Intervascular S.A.S. Zone Industrielle Athelia I La Ciotat Cedex France·Product code DSY·December 9, 2009