BEUDAMED
    35 results · 29ms · Sources: EU EUDAMED, US FDA

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    ULTRAEDGE KERATOME BLADE, MODEL 374803 - ACS

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·40677964011045·Endo Carry-On Procedure Kit includes Intercept ...

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001144·artVeneer life upper anteriors, BIS, A4

    AtriCure Isolator Synergy EnCompass Clamp and Guide System

    FDA UDI
    ATRICURE, INC.·10840143904127·Surgical Ablation System Open, Standard Jaw wit...

    TruFlex™

    FDA UDI
    Ortho Organizers, Inc.·00190707126933·TRUFLEX NiTi Thermal Lower 17x25 (10pk)

    TruFlex

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730015181·NiTi Thermal Lower 17x25 10 archwires per pack

    Alleset

    FDA UDI
    GRI Medical & Electronic Technology Co., Ltd.·16931918197302·Femoral Angiography Drape_W/ windows_87inx125in...

    Alleset

    FDA UDI
    GRI Medical & Electronic Technology Co., Ltd.·16931918178394·Femoral Angiography Drape_W/ windows_87inx125in...

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·March 18, 2025

    ACME SPINE SYSTEM - SERIES 6000, 7000, MONOAXIAL AND POLYAXIAL SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NIPRO INSULIN SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·November 11, 2024

    ATRICURE ISOLATOR SYNERGY ENCOMPASS CLAMP

    FDA Adverse Event
    Malfunction ·ATRICURE, INC.·Product code OCL·January 31, 2025

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·March 18, 2025

    MINIMED QUICK SET INFUSION SET (SC1)

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 27, 2025

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·December 12, 2024

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·December 28, 2025

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·December 11, 2025

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·June 11, 2025

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·May 7, 2025