BEUDAMED
    12 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 ×

    RELEASE 2 OF PHILIPS INTEGRIS SERIES (V5000, BV5000, H5000, BH5000, HM2000) SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Radiology

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984545·anteriors; shade C4; mould R 51

    MEGA PLUS MIS SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809665587053·MIS Cannulated Screw M, Ø4.5 x 45mm, Ø6.0mm Rod

    DELFIA (TM) HIGE KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    FORCE GSU TM SYSTEM AND FORCE GSU TM HANDSET

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    IMP CBL DIA2 SS CABLE SLEEVE

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code JDQ·November 18, 2016

    IMP CBL DIA2 SS CABLE SLEEVE

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code JDQ·November 18, 2016

    IMP CBL DIA2 SS &CABLE SLEEV

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code JDQ·November 30, 2016

    IMP CBL DIA2 SS & CABLE SLEEVE

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code JDQ·July 20, 2016

    DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 28, 2013

    UNKNOWN DEPUY LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·January 28, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 6, 2014