BEUDAMED
    22 results · 27ms · Sources: EU EUDAMED, US FDA

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    EUROIMMUN ANTI-PR3-HN-HR ELISA (IGG)

    FDA 510(k)
    FDA Class 2 ·Immunology

    Best Medical International

    FDA UDI
    BEST MEDICAL INTERNATIONAL, INC.·00841365104404·

    Rebar

    FDA UDI
    Micro Therapeutics, Inc.·00836462002210·027 Micro Catheter

    RebarTM

    FDA UDI
    Micro Therapeutics, Inc.·00847536026872·MICRO CATH 105-5082-130 V01 REBAR

    Rebar

    FDA UDI
    Micro Therapeutics, Inc.·00763000539351·MICRO CATHETER 105-5082-130 V08

    NIR BILIARY STENT

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

    ATTAIN LDS 6216 LEFT-HEART DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NEXIVA 22GA 1.00IN Y

    FDA Adverse Event
    Malfunction ·Product code FOZ·August 10, 2021

    REFLEX CATHETER

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code DQY·March 11, 2025

    STEM EXTRACTOR F/GUIDE BAR 03.401.070

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWB·April 29, 2013

    X-SMART

    FDA Adverse Event
    Malfunction ·DENTSPLY MAILLEFER·Product code LQY·April 27, 2011

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·May 22, 2008

    BD NEXIVA¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 24, 2021

    REBAR

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·May 13, 2024

    REBAR

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·September 26, 2024

    PUMP 1886 780G OUS BLE PUMP MG/DL

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·May 16, 2024

    REBAR

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·May 13, 2024

    SOLITAIRE FR

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·June 26, 2025

    REBAR

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·March 11, 2025

    Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026