BEUDAMED
    25 results · 25ms · Sources: EU EUDAMED, US FDA

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    EVOS Straight Proximal Humerus 7-15 hole Plates (137-225mm)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FAC-4 - Duke Power Cabinet

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588015293·FAC-4 - Duke Power Cabinet

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383512121·"An absorbent paper points is an endodontic pap...

    APPLE ECG (ELECTROCARDIOGRAPH) APP

    FDA Adverse Event
    Injury ·APPLE INC.·Product code QDA·July 5, 2023

    FOTONA FIDELIS ER: YAG LASER SYSTEM AND ACCESORIES

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SECTRA OSTEOPOROSIS PACKAGE

    FDA 510(k)
    FDA Class 2 ·Radiology

    MOSAIC AORTIC BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·November 14, 2017

    HANCOCK II AORTIC BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·November 14, 2017

    530G INSULIN PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·February 6, 2015

    RESTORE PRIME ADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·October 17, 2008

    EON MINI RECHARGEABLE IPG

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·August 4, 2011

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·July 2, 2013

    COREVALVE TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·November 14, 2017

    UNKNOWN EDM CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·September 15, 2016

    HANCOCK II AORTIC BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·September 11, 2017

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DXY·July 22, 2015

    PRESSUREWIRE?

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, COSTA RICA LTDA·Product code DXO·May 27, 2015

    NEU_ENTERRA_INS

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LNQ·February 7, 2017

    DEPUY ASR XL FEM IMP SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·August 13, 2015

    INTERVERTEBRAL FUSION DEVICE W/INTEGRATED FIXATION, LUMBAR

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code OVD·March 14, 2018