BEUDAMED
    25 results · 38ms · 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 ×

    PNEUMOCLEAR

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

    AGXO

    FDA UDI
    Oticon A/S·05707131356680·G400 S, MINIRITE R LI-ION 2.4G C063 AGXO

    Dornier MedTech

    FDA UDI
    DORNIER MEDTECH AMERICA, INC.·04049958003103·270 micron Holmium Laser Fiber Cable, Single Us...

    Dornier MedTech

    FDA UDI
    DORNIER MEDTECH AMERICA, INC.·00810116023271·270 Micron SU Thulio Slim Performance 3m Fiber

    AVANOS

    FDA UDI
    Avanos Medical, Inc.·00350770456928·CORFLO* Nasogastric/Nasointestinal Feeding Tube

    CORFLO ULTRA Lite NG

    FDA UDI
    CORPAK MEDSYSTEMS, INC.·10815149023059·Feeding tube, non weighted

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383534512·"An absorbent paper points is an endodontic pap...

    Halyard

    FDA UDI
    Avanos Medical, Inc.·10680651456929·HALYARD* CORFLO* Nasogastric/Nasointestinal Fee...

    JILCO TRACTION-FLEXION CHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    REEFLEX PTA CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SILK SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Death ·ETHICON INC.·Product code GAP·July 17, 2018

    SILK SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAP·July 17, 2018

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·October 27, 2020

    OT VERIO TEST STRIPS

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 27, 2014

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·June 26, 2013

    INSYNC MAXIMO

    FDA Adverse Event
    Malfunction ·MEDTRONIC S.A.·Product code NIK·August 11, 2011

    BD PEGASUS PNK 20GA X 1.16IN PRN-CAP Y

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·August 31, 2022

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MRU·November 26, 2013

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MRU·November 26, 2013

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·January 5, 2018