BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    ULTRACUFF BLOOD PRESSURE CUFF AND INFLATION BAG

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BIFURCATED GORE TEX STRETCH VASCULAR GRAFT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PREVIEW XT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INVIVO CORPORATION MRI PT MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·INVIVO CORPORATION·Product code MWI·January 9, 2013

    UNK DEPUY AML CEMENTED STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWY·January 5, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 24, 2014

    TO GORE-TEX® STRETCH VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021

    GORE-TEX® STRETCH VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021

    GORE-TEX® STRETCH VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021