BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    VACUETTE MULTIPLE SAMPLE LUER ADAPTER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981619·anteriors; shade A3.5 light; mould UM6

    PACING LEAD MODELS SA, 350, SAM 500

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    CHROMOLITE EP

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

    ION PACLITAXEL-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·February 27, 2013

    D/M H-GRIP INTRODUCER

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·January 12, 2011

    1.85MM X 16MM FLUTED ROUTER

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·December 18, 2013

    CONNECTOR, 1/4" X 1/4" STRAIGHT WITH LUER LOCK PORT

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code OEZ·April 26, 2016

    Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 722005 The device is an X-Ray Generator.

    FDA Enforcement
    Class II ·Terminated·Philips North America, LLC·March 25, 2020