BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Hexalux Examination Light (MG-MF)

    Reg #: 3003950207 · FEI: 3003950207 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    6
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    STERIS Corporation
    Registration Number
    3003950207
    FEI Number
    3003950207
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    6100 Heisley Rd
    City
    Mentor
    State
    OH
    ZIP
    44060
    Country
    US

    Owner / Operator

    Firm Name
    STERIS Corporation
    Operator Number
    10078069
    Address
    5960 Heisley Road
    City
    Mentor
    State
    OH
    Postal Code
    44060
    Country
    US

    Products

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

    Proprietary Names

    Hexalux Examination Light (MG-MF) Hexalux Mobile Stand (MG-MF) AMSCO LD202 Wall Controller (MG-CFE) AMSCO LD202 In-Ceiling Lighting System (MG-CFE) LED202 In-Ceiling Single Lighting System (MG-MF) LED202 In-Ceiling Dual Lighting System (MG-MF)

    Establishment Types

    Repack or Relabel Medical Device