BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    21HQ513D

    FDA 510(k)
    FDA Class 2 ·Radiology

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776165956·PRYOR PEAN RETRACTOR . BLADE

    PILLING

    FDA UDI
    TELEFLEX INCORPORATED·24026704514322·

    BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code QJR·August 9, 2021

    Alteon

    FDA UDI
    Exactech, Inc.·10885862517692·ALTEON MONO REVSTM TRIAL SIZE 21X295

    HUMAN IGG SUBCLASS LIQUID REAGENT KITS, PRODUCT CODE NK001.T

    FDA 510(k)
    FDA Class 2 ·Immunology

    CORE 3D ABUTMENT SYSTEM FOR DIGITAL PROSTHETIC SOLUTIONS

    FDA 510(k)
    FDA Class 2 ·Dental

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 30, 2014

    N/A

    FDA Adverse Event
    Malfunction ·Product code JOH·August 15, 2011

    GYNECARE TVT SECUR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code PAH·July 9, 2013

    DRX Revolution Mobile X-Ray System

    FDA Enforcement
    Class II ·Ongoing·Carestream Health, Inc.·December 13, 2023