BEUDAMED
    12 results · 27ms · Sources: EU EUDAMED, US FDA

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    BRAINSPACE Inc

    FDA registration
    BRAINSPACE Inc·2 products·🇺🇸 United States

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·December 16, 2014

    BRAINSPEC, INC

    FDA registration
    BRAINSPEC, INC·2 products·🇺🇸 United States

    BrainSpec Core™ Software

    FDA UDI
    BrainSpec Inc.·00860013965204·BrainSpec Core™ Software is a web-based softwar...

    BrainSpec Core™ Software

    FDA UDI
    BrainSpec Inc.·00198715251623·BrainSpec Core™ Software is a web-based softwar...

    BrainSpec Core™ Software

    FDA 510(k)
    FDA Class 2 ·Radiology

    Retainer Braun Space

    Device
    EU MDR · Eu Md Class 1 ·Bucher Leichtbau AG·On the market

    Retainer Braun Space

    Device
    EU MDR · Eu Md Class 1 ·Bucher Leichtbau AG·On the market

    PROGREAT

    FDA Adverse Event
    Malfunction ·TERUMO CLINICAL SUPPLY CO., LTD.·Product code DQO·July 28, 2022

    B BRAUN SPACE PUMP

    FDA Adverse Event
    Malfunction ·B BRAUN·Product code FRN·February 17, 2012

    MRI /LEGACY NEUROSURGERY AND BRAIN SPEC

    FDA Adverse Event
    Injury ·UNKNOWN·Product code LNH·April 3, 2025

    SILICONE IMPLANT

    FDA Adverse Event
    Injury ·UNK·Product code FTR·January 29, 2019