BEUDAMED
    FDA Registration Active 🇨🇭 Switzerland

    Multiple Navigator

    Reg #: 1000312377 · FEI: 1000312377 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    24
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    Derungs Licht AG
    Registration Number
    1000312377
    FEI Number
    1000312377
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Hofmattrasse 12
    City
    Gossau Sankt Gallen
    Country
    CH

    Owner / Operator

    Firm Name
    HERBERT WALDMANN GMBH & CO.
    Operator Number
    8010699
    Address
    9 W Century Dr
    City
    Wheeling
    State
    IL
    Postal Code
    60090
    Country
    US

    Products

    Device Name Product Code
    Device, Medical Examination, Ac Powered KZF

    Proprietary Names

    Multiple Navigator Multiple Halux I Multiple Halux N50 Multiple Tevisio Multiple Polaris Multiple TR7 Multiple Stellar Multiple Crescent Multiple Triango 30 Multiple Triango 80 Multiple MLD Multiple Visiano 10-1 Multiple Omnivue Multiple Halux N30 Multiple Zera Multiple Triango 100 Multiple Stellar Duo Multiple Visiano 20-2 Multiple Halux III Multiple Opticlux Multiple Taneo Multiple Amadea Multiple WLA Multiple ALD

    Establishment Types

    Manufacture Medical Device Manufacture Medical Device for Another Party (Contract Manufacturer)