BEUDAMED
    44 results · 23ms · Sources: EU EUDAMED, US FDA

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    RxSight Contact Lens

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Philips

    FDA UDI
    Sbo Hearing A/S·05714464002795·HEARLINK 5010 FW 1.0

    NA

    FDA UDI
    Stryker GmbH·07613154639700·Screw Marker 19,9

    Universal electrode patch

    FDA UDI
    BRAEMAR MANUFACTURING, LLC·B146PE30·

    ALINITY I PROCESSING MODULE

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·March 17, 2022

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68120190900090·9mm LG Lordotic Expanding Trial, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68120190900130·13mm LG Lordotic Expanding Trial, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68120190900100·10mm LG Lordotic Expanding Trial, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68120190900120·12mm LG Lordotic Expanding Trial, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68120190900070·7mm LG Lordotic Expanding Trial, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68120190900140·14mm LG Lordotic Expanding Trial, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68120190900080·8mm LG Lordotic Expanding Trial, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68120190900110·11mm LG Lordotic Expanding Trial, HiJAK™ Cervical

    PLAINSENSE WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    EXACTECH EQUINOXE, PLATFORM FRACTURE STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARCHITECT I1000SR

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·July 26, 2022

    ARCHITECT I2000 ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code NIG·August 21, 2013

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·July 2, 2019

    DESARA

    FDA Adverse Event
    Injury ·CALDERA MEDICAL, INC.·Product code FTL·October 20, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011