BEUDAMED
    FDA Registration Active 🇦🇹 Austria

    M5Sc-D

    Reg #: 8020021 · FEI: 3004377820 · Expires 2025
    View on FDA
    Products
    3
    Proprietary Names
    32
    Establishment Types
    1
    Classifications
    3

    Registration Details

    Registration Name
    GE Healthcare Austria GmbH & Co OG
    Registration Number
    8020021
    FEI Number
    3004377820
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    TIEFENBACH 15
    City
    ZIPF Oberosterreich
    Country
    AT

    Regulatory Submissions

    510(k) Number
    K231989

    Owner / Operator

    Firm Name
    GE HealthCare Technologies Inc.
    Operator Number
    9912004
    Address
    3000 N. Grandview Blvd
    City
    Waukesha
    State
    WI
    Postal Code
    53188
    Country
    US

    US Agent

    Business Name
    GE HealthCare Technologies, Inc
    Contact Name
    Tracey Holevas
    Address
    3000 N. Grandview BLVD
    City
    Waukesha
    State
    WI
    ZIP
    53188
    Country
    US
    Email
    [email protected]
    Phone
    262 3092157

    Products

    Device Name Product Code
    System, Imaging, Pulsed Doppler, Ultrasonic IYN
    Transducer, Ultrasonic, Diagnostic ITX
    System, Imaging, Pulsed Echo, Ultrasonic IYO

    Proprietary Names

    M5Sc-D LOGIQ E10s ML4-20-D 6Tc-RS L3-12-D LOGIQ Fortris R3 to R4 SW Upgrade W ML6-15-D C3-10-D LOGIQ Fortris R3 to R4 HW Upgrade W LOGIQ E10s R2R3 to R4 SW Upgrade W LOGIQ E10s R2R3 to R4 SW Upgrade 6S-D C1-6VN-D RIC5-9-D P2D C2-9VN-D LOGIQ E10s R2R3 to R4 HW Upgrade LOGIQ Fortris R3 to R4 SW Upgrade IC5-9-D BE9CS-D L4-20t-D LOGIQ Fortis L2-9-D L2-9VN-D ML4-20VN-D RAB6-D C1-6-D L8-18i-D LOGIQ E10s R2R3 to R4 HW Upgrade W P6D C2-9-D LOGIQ Fortris R3 to R4 HW Upgrade

    Establishment Types

    Manufacture Medical Device