BEUDAMED
    10 results · 31ms · Sources: EU EUDAMED, US FDA

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    BRIGHTWAY BRAND LATEX SURGICAL GLOVES - STERILE (POWDER FREE)

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113189·STERILIZING CASE SMALL KATENA IOP

    CRYOVALVE SG PULMONARY HUMAN HEART VALVE (AND CONDUIT)

    FDA 510(k)
    FDA Unclassified ·Unknown

    NCB Polyaxial Locking Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RADIFOCUS OPTITORQUE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 13, 2022

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·March 7, 2013

    MANUAL ORTHOPEDIC SURGICAL INSTRUMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK INSTRUMENT MANUFACTURING·Product code LXH·February 15, 2011

    ATTAIN ABILITY PLUS MRI SURESCAN

    FDA Adverse Event
    Injury ·MPRI·Product code OJX·August 8, 2014

    METRX SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HRX·June 10, 2024

    OPTITORQUE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Malfunction ·Product code DQO·January 20, 2021