BEUDAMED
    23 results · 25ms · Sources: EU EUDAMED, US FDA

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    Amendia Interbody Fusion Devices

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169502192·INTERBODY 2151310 LARGE - 6 DEG 10MM

    CR MULTIFORMAT READER

    FDA UDI
    AGFA·05414904160480·CR MULTIFORMAT READER

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100295·FRANKEL INFANT EYE SPECULUM

    Flextrode

    FDA UDI
    COSMAN MEDICAL, LLC·08132500133826·Electrode 15cm, 13mm Tip, 20G

    NA

    FDA UDI
    BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·00813250013382·Flextrode, 15cm,17G Introducer

    HNM SPORTS MEDICINE

    FDA UDI
    HNM STAINLESS, LLC.·00842962101551·ETHOS PRO LABRAL ANCHOR, PEEK, 3.3mm x 6mm, (2)...

    PLC SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VU APOD INTERVERTEBRAL BODY FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HNM SPORTS MEDICINE

    FDA UDI
    HNM STAINLESS, LLC.·00842962103623·ETHOS PRO LABRAL ANCHOR, PEEK, 3.3mm x 6mm, (2)...

    GMK-PRIMARY FEMUR PS CEMENTED SIZE 6 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 16, 2020

    GMK-PRIMARY FEMUR PS CEMENTED SIZE 4

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·May 22, 2019

    GMK-PRIMARY FEMUR PS CEMENTED SIZE 4 LEFT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·August 23, 2017

    GMK-PRIMARY FEMUR PS CEMENTED SIZE 6 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 25, 2018

    INTELLIVUE MULTI-MEASUREMENT MODULE X3

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·June 12, 2025

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 7, 2013

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·June 7, 2011

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code NIQ·September 4, 2008

    INTERSTIM

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·July 11, 2024

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·March 20, 2025