BEUDAMED
    21 results · 24ms · Sources: EU EUDAMED, US FDA

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    Adaptix Interbody System with Titan nanoLOCK Surface Technology

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    10PW - Penn Power & Light

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588012179·10PW - Penn Power & Light

    PREMIO 10 MOXA

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    GE SYSTEM FIVE

    FDA 510(k)
    FDA Class 2 ·Radiology

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·December 30, 2010

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 12, 2024

    GORE® TAG® THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·January 12, 2016

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·October 17, 2012

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·October 17, 2012

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·October 17, 2012

    ATTAIN ABILITY

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OJX·December 9, 2013

    TITANIUM ABUTMENT 6 MMH COMPATIBLE WITH: STRAUMANN® BONE LEVEL RC

    FDA Adverse Event
    Malfunction ·PRISMATIK DENTALCRAFT, INC.·Product code NHA·October 27, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLCL)·Product code JAA·August 3, 2011

    TAXUS® LIBERTÉ®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·July 2, 2013

    BD VENFLON¿ PRO SAFETY PERIPHERAL SAFETY IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·December 9, 2022

    UNKNOWN RIGHT HIP - REJUVENATE/ABGII NECK

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code MEH·January 13, 2014

    RAPIDEC CARBA NP

    FDA Adverse Event
    Malfunction ·BIOMÉRIEUX, SA·Product code PTJ·September 2, 2020

    COOK AIRWAY EXCHANGE CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code LRC·June 16, 2017

    ZILVER PTX 35 DRUG-ELUTING STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIU·February 1, 2022

    ZILVER PTX DRUG-ELUTING PERIPHERAL STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIU·February 1, 2022