BEUDAMED
    13 results · 27ms · Sources: EU EUDAMED, US FDA

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    MITEK ROTATOR CUFF QUICKANCHOR PLUS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CAPSTONE PTC™ Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169187412·SPACER 3992611 26MM X 11MM

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198826·AK3 Ultra Insert Trial Size 6, 11mm

    Buccal Tubes

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746084126·DB TUBE INCONEL UL 2ND MOL 022 T-15 R=0 2MM

    SONARMED AIRWAY MONITORING SYSTEM, MODEL 0901

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Cuffix

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    STANDARD INSERTION HANDLE

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·December 26, 2019

    CAPSTONE PTC¿ SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code MAX·February 7, 2025

    ASR ACETABULAR IMPLANT 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·March 7, 2013

    EXCELLENCE PS+

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    CONSULTA CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 8, 2014

    STANDARD INSERTION HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code LXH·February 26, 2016

    RECON LOCKING AIMING ARM FOR LATERAL ENTRY FEMORAL NAILS-EX

    FDA Adverse Event
    Malfunction ·SYNTHES BRANDYWINE·Product code FZX·February 26, 2016