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

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    SENTIO MMG

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517565204·CoRoent Ant TLIF PEEK, 13x11x30mm 4°

    COE-FLEX®

    FDA UDI
    Gc America Inc.·D6581313041·COE-FLEX® s Heavy Body (catalyst only) (1 x 45m...

    COE-FLEX®

    FDA UDI
    Gc America Inc.·10386040004947·COE-FLEX® s Heavy Body (catalyst only) (1 x 45m...

    OPTIMA XR120

    FDA 510(k)
    FDA Class 2 ·Radiology

    SYDNEY IVF PVP

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    THERMOCOOL® SF NAV BI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 12, 2013

    THERMOCOOL® SF NAV UNI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·May 16, 2013

    VERSAFITCUP CC CANCELLOUS BONE SCREW

    FDA Adverse Event
    MEDACTA INTERNATIONAL, SA·Product code LZO·May 14, 2014

    STOCKERT 70 RF GENERATOR

    FDA Adverse Event
    Injury ·STOCKERT GMBH·Product code DRF·April 16, 2013

    PELVICOL 2CM X 7C, 1.0MM

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TISSUE SCIENCE LABORATORIES·Product code FTL·May 17, 2013

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·October 1, 2014

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 16, 2011

    O-Ring Abutment 4.1mm(D) x 2mm(H) Item: OSO20 Dental implants

    FDA Enforcement
    Class II ·Terminated·Biomet 3i, LLC·August 24, 2016

    3.2MM Pellet Insertion Tray Catalog Number: B9743

    FDA Enforcement
    Class II ·Terminated·Busse Hospital Disposables, Inc.·June 8, 2022

    8110 ALARIS SYRINGE PUMP

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·December 16, 2020

    STOCKERT 70 RF GENERATOR

    FDA Adverse Event
    Injury ·STOCKERT GMBH·Product code DRF·August 22, 2013

    ADVANCE 35 LP LOW PROFILE BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·February 3, 2017

    ADVANCE 35 LP LOW PROFILE BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·March 10, 2017

    STOCKERT 70 RF GENERATOR

    FDA Adverse Event
    Injury ·STOCKERT GMBH·Product code DRF·July 14, 2016