BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    HEART-LIFT BALLOON POSITIONER

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    Centricity Universal Viewer

    FDA 510(k)
    FDA Class 2 ·Radiology

    REOSS POWDER, REOSS PUTTY, REOSS GEL, MODELS R-1,RP-1, RG-1

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·January 25, 2013

    FLEXHD - 8CM X 16CM

    FDA Adverse Event
    MTF·Product code GAT·January 14, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 6, 2014

    BW Webster Duo-Decapolar, Product Number D728260RT; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026