BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Conventional Laryngoscope Blade

    Reg #: 1314417 · FEI: 1314417 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    19
    Establishment Types
    3
    Classifications
    1

    Registration Details

    Registration Name
    SunMed Group Holdings, LLC dba AirLife
    Registration Number
    1314417
    FEI Number
    1314417
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    2710 Northridge Dr NW Ste A
    City
    Grand Rapids
    State
    MI
    ZIP
    49544
    Country
    US

    Owner / Operator

    Firm Name
    SunMed Group Holdings, LLC dba AirLife
    Operator Number
    10044795
    Address
    2710 Northridge Drive NW, Suite A
    City
    Grand Rapids
    State
    MI
    Postal Code
    49544
    Country
    US
    Correspondent
    Rob Yamashita

    Products

    Device Name Product Code
    Laryngoscope, Rigid CCW

    Proprietary Names

    Conventional Laryngoscope Blade Conventional Laryngoscope Handle GreenLine® Disposable Fiber Optic Laryngoscope Blade GreenLine®/D™ LED Conventional Laryngoscope Handle GreenLine®/D™ Fiber Optic Laryngoscope Handle Fiber Optic Laryngoscope Blade GreenLine® Fiber Optic Laryngoscope Blade GreenLine®/D™ LED Disposable Laryngoscope Handle GreenLine® Fiber Optic Laryngoscope Handle GreenLine®/D™ LED Laryngoscope Blade Conventional Disposable Laryngoscope Handle GreenLine®/D™ Fiber Optic Laryngoscope Blade SunOne™ System Laryngoscope Blade SunOne™ System Laryngoscope Handle GreenLine® Disposable Fiber Optic Laryngoscope Handle Fiber Optic Laryngoscope Handle Conventional Disposable Laryngoscope Blade Blade, Laryn, Vs, Plastic, Mac 2 Blade, Laryn, Vs, Plastic, Mil 2 & 3

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility