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

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    VICRYL RAPIDE SUTURE

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

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377073150·RELINE C Ti Rod, 4.0x110mm Pre Bent

    SwishActive™ Implant

    FDA UDI
    IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307106661·Ø3.7 x 8 Platform 3.5mmD

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690191124·AK3 Flat Insert Trial Size 1-3 - 10mm

    GRASPING FORCEPS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    XTRACETEZE SURGICAL SKIN STAPLE REMOVER 2001

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    METRX® SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HRX·July 17, 2025

    FIBER ONE

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·December 29, 2010

    SPACEMAKER BLUNT TIP TROCAR 10MM

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY USSC·Product code GCJ·January 9, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 18, 2014

    Type S Extension For use with Varian, CIVCO, Prescription Only - Product Usage: Device is intended for patient positioning.

    FDA Enforcement
    Class II ·Terminated·Med Tec Inc·June 10, 2020