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

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    GE DISCOVERY ST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    CD HORIZON® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074364452·CONECTOR 7041220 CLSLAT 20MM TI 4.5/6.35

    Sentient Manufacturing

    FDA UDI
    Sentient Manufacturing, LLC·00860007603730·Laser Fiber Cannula 8" - 200 mm

    Advanced Shield Hydrogel Silver Wound Barrier GEL, 2oz Tube

    FDA UDI
    Kericure Inc.·00858071004348·Advanced Shield Hydrogel Wound Barrier with Sil...

    Ophthalmic Scissors

    FDA UDI
    KATENA PRODUCTS, INC.·00841668105115·TROUTMAN-CASTROVIEJO SCISSORS RIGHT

    Entuit Thrive

    FDA UDI
    XERIDIEM MEDICAL DEVICES, INC.·00827002356184·Entuit Gastrostomy BR Balloon Retention Feeding...

    ENDOPATH SURESEAL REDUCER CAP

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    LEVEEN REFLECT MONOPOLAR/BIPOLAR NEEDLE ELECTRODE

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

    BD® PLASTIC NRFIT¿ SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code QEH·September 9, 2022

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867462021·Dilator, 4.1 x 220mm

    DILATOR, 4.1 X 220MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·May 21, 2026

    BD SYRINGE NRFIT¿ LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code QEH·May 17, 2024

    SYRINGE 10ML L/T SSU NRFIT WWS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code QEH·December 22, 2024

    DILATOR, 4.1 X 220MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HNW·October 29, 2024

    DILATOR, 6.0 X 200MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HNW·December 2, 2024

    DILATOR, 6.0 X 200MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HNW·October 29, 2024

    DILATOR, 7.1 X 190MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HNW·October 29, 2024

    DILATOR, 7.1 X 190MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HNW·November 26, 2024

    DILATOR, 5.1 X 210MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HNW·December 2, 2024

    DILATOR, 5.1 X 210MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HNW·October 29, 2024