BEUDAMED
    12 results · 20ms · 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 ×

    FUKUDA DENSHI FF SONIC UF-5800 GENERAL PURPOSE ULTRASOUND SCANNING SYSTEM WITH DOPPLER

    FDA 510(k)
    FDA Class 2 ·Radiology

    Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR79904011·Sprint II Bracket McLaugh/Benn/Trev. .022" max....

    Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR79904010051·Sprint II Bracket McLaugh/Benn/Trev. .022" max....

    Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR79904011001·Sprint II Bracket McLaugh/Benn/Trev. .022" max....

    Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR79904010101·Sprint II Bracket McLaugh/Benn/Trev. .022" max....

    NA

    FDA UDI
    STRYKER CORPORATION·07613327064032·Resectoscope Working Element, Passive, 22/24 Fr.

    ORTHOSS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MAMBA and MAMBA Flex Microcatheters

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MAMBA? FLEX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQY·September 11, 2025

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 5, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011

    ATTAIN ABILITY

    FDA Adverse Event
    Malfunction ·MPRI·Product code OJX·August 7, 2014