BEUDAMED
    82 results · 26ms · Sources: EU EUDAMED, US FDA

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    Nalu Neurostimulation SCS system

    FDA 510(k)
    FDA Class 2 ·Neurology

    EarQ

    FDA UDI
    Oticon A/S·05707131357120·G30 S, MINIRITE R LI-ION 2.4G C063 EARQ

    NA

    FDA UDI
    Synthes GmbH·10886982142078·2.4MM CORTEX SCREW SELF-TAPPING/18MM

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383554565·"An absorbent paper points is an endodontic pap...

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383512527·"An absorbent paper points is an endodontic pap...

    HydroSens A (hioxifilcon A) Spherical Hydrogel Soft Contact Lens

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    OSA RIGID INTERNAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    ASCENDA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·February 24, 2016

    INDURA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·February 24, 2016

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·February 24, 2016

    STRATTICE

    FDA Adverse Event
    Injury ·LIFECELL CORPORATION·Product code FTM·August 28, 2016

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·June 15, 2017

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 12, 2024

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·July 3, 2018

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·November 21, 2016

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·July 23, 2019

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·July 23, 2019

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·August 4, 2011

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·October 27, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 2, 2013