BEUDAMED
    10,000 results · 80ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    UNKNOWN·Product code ITJ·September 5, 2014

    TDXSP ELECTRIC RED EURO WIDE BASE W/ 23-1 SSD GEAR BOX

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·April 5, 2016

    WAVELIGHT EX500 EXCIMER LASER

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·July 31, 2020

    TRILOGY O2 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·November 19, 2023

    COLORED CONTACT LENS

    FDA Adverse Event
    Injury ·UNK·Product code KYE·February 28, 2018

    SPACEMAKER

    FDA Adverse Event
    Injury ·COVIDIEN·Product code GCJ·May 5, 2026

    TRAILBLAZER

    FDA Adverse Event
    Injury ·COVIDIEN·Product code DQY·February 1, 2017

    HEMOSPLIT CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code MSD·December 16, 2024

    PDS LL PLUS ANTIBACTERIAL SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·October 6, 2021

    VICRYL PLUS POLYGLACTIN 910 SUTURE UNKNOWN PROD

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·October 6, 2021

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·December 12, 2021

    DERMABOND ADVANCED UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code MPN·October 6, 2021

    LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·August 20, 2020

    LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·September 26, 2020

    UNKNOWN

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code DTK·December 29, 2016

    UNKNOWN KNEE TIBIAL TRAY

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 20, 2019

    Inserter/Remover Contact Lens

    FDA classification
    FDA Class 1 ·Inserter/Remover Contact Lens

    Laser Safety Goggles (Sport Frame)

    FDA UDI
    AMD Lasers·00851759007167·Laser Safety Sport Goggle, OD 5+ @ 800nm-820nm ...

    ZIIP Beauty

    FDA UDI
    ZIIP, INC.·00851367006224·ZIIP EYES Kit

    MAXI EYE

    FDA registration
    MAXI EYE·1 product·🇰🇷 South Korea