BEUDAMED
    160 results · 24ms · Sources: EU EUDAMED, US FDA

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    Activmotion S DTO

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814541·GENUMEDI SAND SIZE III

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694041621·2.4mm Distractor/Compression Pin

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112687·BARRON CORNEAL PUNCH 9.25MM

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112724·BARRON VACUUM PUNCH 6.75MM

    WATERLASE FOR APICOECTOMY

    FDA 510(k)
    FDA Class 2 ·Dental

    THE O'NEIL STERILE FIELD URINARY CATHETER KIT

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

    GORE EXCLUDER CONF AAA ENDO - TRUNK-IPSILATERAL

    FDA Adverse Event
    Malfunction ·W. L. GORE ASSOCIATES, INC.·Product code MIH·November 26, 2025

    DUET EXTERNAL DRAINAGE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code PCB·November 18, 2025

    BD ALARIS PUMP INFUSION SET

    FDA Adverse Event
    Malfunction ·BD / BD SWITZERLAND SÀRL·Product code FPA·June 17, 2025

    CRE¿ PRO

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·July 9, 2025

    PUMP INFUSION SET IV TUBING/ACCESSORIES

    FDA Adverse Event
    Malfunction ·BD SWITZERLAND SARL·Product code FPA·August 11, 2025

    GMK-REVISION REVISION FIXED TIBIAL TRAY CEMENTED SIZE 5 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·August 2, 2024

    PENUMBRA ASPIRATION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code QEX·September 25, 2023

    PCA IV TUBING

    FDA Adverse Event
    Injury ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·August 26, 2025

    CADD EXTENSION SET

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·November 8, 2023

    BALL HEADS: COCR 01.25.031 COCR BALL HEAD 12/14 Ø 36 SIZE M 0

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·December 21, 2023

    BD LUER-LOK¿ STERILE, SINGLE USE SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·August 15, 2023

    SHOULDER SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·September 4, 2025

    3.5 MM LOCKING SCREW

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·October 17, 2008