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.

    OXYGEN MONITOR OHIO 5100

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    REPICCI LOCKED KEEL TIBIAL BEARING

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FASTBRACES CERAMIC BRACKETS

    FDA 510(k)
    FDA Class 2 ·Dental

    SURGICAL GUT SUTURE - CHROMIC

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAL·May 23, 2014

    POWER PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·October 10, 2012

    DURATA STS OPTIM ACTIVE FIXATION, SJ4 CONNECTOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 10, 2010

    Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018