BEUDAMED
    23 results · 22ms · Sources: EU EUDAMED, US FDA

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    Game Ready GRPro 2.1 System

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    ECHO BI-METRIC HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304462892·

    Echo® Bi-Metric® Hip System

    FDA UDI
    Biomet Orthopedics, LLC·00887868260605·

    Aspida

    FDA UDI
    ALPHATEC SPINE, INC.·00840967190945·LUMBAR DTS GUIDE 14MM

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198451·AK3 Ultra Insert Trial Size 1, 14mm

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776199388·LLETZ Allis Tissue Forcep

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123083·K-WIRE - DOUBLE TROCAR 1.1mm DIA x 100mm

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780419068·Integra® Miltex® House Crimper Forceps 3-3/8" S...

    MAQUET FLOW-I C20, MAQUET FLOW-I C30, MAQUET FLOW-I C40

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MEDRANGE ELECTROSURGICAL GENERATOR

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

    Responsive Orthopedics Total Knee Arthroplasty System

    FDA UDI
    RESPONSIVE ORTHOPEDICS, LLC·00841973107934·TRIAL 90-SRK-192114 POLY-MPCS 1X14 LEFT

    BD PHOENIX PANEL NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·December 12, 2023

    BD PHOENIX PANEL NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·December 12, 2023

    BD PHOENIX PANEL NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·December 12, 2023

    BD PHOENIX PANEL NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·December 12, 2023

    BD PHOENIX PANEL NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·December 12, 2023

    POUNCE VENOUS THROMBECTOMY SYSTEM

    FDA Adverse Event
    Injury ·SURMODICS INC·Product code QEW·May 16, 2024

    ARDIS INSERTER

    FDA Adverse Event
    Injury ·ABBOTT SPINE·Product code LXH·October 7, 2008

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 20, 2013

    PROTECTA CRT-D

    FDA Adverse Event
    Death ·MEDTRONIC MED REL, INC.·Product code NIK·August 4, 2011