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

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    PRE-SURE

    FDA 510(k)
    FDA Class 2 ·Radiology

    CODMAN

    FDA UDI
    Cerenovus, Inc.·10886704002338·CODMAN Slimline Mini Aneurysm Clip No 7 Forward...

    Conventional Lead Apron .5mm Medium 24 X 39

    FDA UDI
    Flow X Ray Corporation·00843696123314·Conventional Lead Apron .5mm Medium 24 X 39, Red

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383549165·"An absorbent paper points is an endodontic pap...

    IRV2000 INDIVIDUAL RECREATIONAL VEHICLE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    BRENNEN MEDICAL SURGICAL MESH, GLUCAMESH/GLUCATEX

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

    HAHN TAPERED IMPLANT Ø4.3 X 11.5 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·October 9, 2025

    HAHN TAPERED IMPLANT Ø4.3 X 11.5 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·March 13, 2025

    ATTUNE MEDIAL DOME PAT 41MM

    FDA Adverse Event
    Malfunction ·DEPUY IRELAND 9616671·Product code JWH·October 15, 2018

    ADVANTA V12 COVERED STENT SYSTEM

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·February 2, 2020

    ADVANTA V12 COVERED STENT SYSTEM

    FDA Adverse Event
    Death ·ATRIUM MEDICAL CORPORATION·Product code NIO·February 2, 2020

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·June 4, 2018

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 27, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 2, 2013

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 19, 2012

    NI

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code JXG·June 27, 2018

    VALIANT CAPTIVIA UNK

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code MIH·December 18, 2019

    GORE® TAG® CONFORMABLE THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·May 11, 2021

    GORE® TAG® CONFORMABLE THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Death ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·May 12, 2021