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

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    O-Genesis Graft Delivery System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377047618·RELINE-O Trial, 10mm H Ang Left L-pop

    Ceramco® iC

    FDA UDI
    Dentsply International Inc.·D00142006060·B1

    Zavation

    FDA UDI
    Zavation LLC·00842166131705·Ti3Z CIF 12mmx14mmx6mm -6 deg

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180172456·ADAPTER, 3MM X 80MM VALTCHEV UTERINE MOBILIZER

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694007269·OSA System Visidisk

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869683753·MOSS Coupler Part 1

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869634380·MOSS VRS MIS Correction Tool

    SYNCHRON SYSTEMS AMPHETAMINE REAGENT

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    NVA-63-8 NEUROVASCULAR ARRAY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    ENDO GIA UNIVERSAL 12MM SINGLE USE INST

    FDA Adverse Event
    Injury ·NORTH HAVEN - USS·Product code GDW·June 29, 2006

    LIGASURE LAPAROSCOPIC SLR/DIV

    FDA Adverse Event
    Malfunction ·VALLEYLAB·Product code GEI·June 8, 2006

    RESTORE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·February 27, 2015

    REVEAL XT

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code DSI·February 8, 2014

    ENRHYTHM

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·August 10, 2013

    PROTECTA XT DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·February 8, 2014

    LIGASURE XTD ELECTRODE

    FDA Adverse Event
    Injury ·VALLEY·Product code GEI·June 12, 2006

    MICROSCAN DRIED POS MIC PANEL TYPE 20A

    FDA Adverse Event
    Malfunction ·DADE BEHRING, INC.·Product code LTT·September 27, 2005

    BIOGX SARS-COV-2 OSR FOR BD MAX SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code QJR·May 13, 2020

    CAPSURE SENSE

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 10, 2013