BEUDAMED
    7 results · 18ms · 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 ×

    KSEA CULDOCENTESIS SET

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    COLLAGEN DENTAL MENBRANE - CONFORMABLE II

    FDA 510(k)
    FDA Class 2 ·Dental

    Kitazato OPU Needles

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    STOPCOCK MANIFOLD GANGS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FMG·June 17, 2020

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 15, 2013

    SCORPIO-FLEX PS TIBIAL TRIAL

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·December 22, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 29, 2014