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

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    RELEASE NF ANTIBACTERIAL FOLEY CATHETER, ANTIBACTERIAL PERSONAL CATHETER

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

    ADVANCE®

    FDA UDI
    Microport Orthopedics Inc.·M684K00141431·

    Select Kit

    FDA UDI
    MEDIVATORS INC.·40677964011021·SELECT KIT includes Endo Carry-on Transport Pad...

    AtriCure Isolator Synergy EnCompass Clamp and Guide System

    FDA UDI
    ATRICURE, INC.·10840143904110·Surgical Ablation System Open, Long Jaw with Gl...

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001143·artVeneer life upper anteriors, BIM, A4

    TruFlex™

    FDA UDI
    Ortho Organizers, Inc.·00190707126926·TRUFLEX NiTi Thermal Lower 16x25 (10pk)

    TruFlex

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730015174·NiTi Thermal Lower 16x25 10 archwires per pack

    MALE LL ADAPTOR

    FDA Adverse Event
    Malfunction ·Product code FPA·May 17, 2021

    SEC 20DP, TEXIUM & HANGER V/NV

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·March 31, 2021

    MIDAS TOUCH NITRILE EXAMINATION GLOVES-POWDERED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    KAWASUMI LABORATORY BLOOD DRAWING KIT

    FDA 510(k)
    FDA Class 2 ·Hematology

    NO MATCH

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWS·September 25, 2025

    0009613348-2023-001143

    FDA Adverse Event
    Injury ·INSTITUT STRAUMANN AG·Product code DZE·January 5, 2023

    WAVEWRITER ALPHA?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·September 5, 2025

    BD LUER-LOCK¿ MALE ADAPTER

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·December 30, 2022

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·January 25, 2026

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·January 25, 2026

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·April 3, 2025

    SEC 20DP, TEXIUM & HANGER V/NV

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·February 11, 2021

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·February 26, 2013