BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Keracel LASIK Corneal Shield

    Reg #: 1211998 · FEI: 1211998 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    25
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    Beaver-Visitec International, Inc.
    Registration Number
    1211998
    FEI Number
    1211998
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    303 Wyman St Ste 350
    City
    Waltham
    State
    MA
    ZIP
    02451
    Country
    US

    Owner / Operator

    Firm Name
    Beaver-Visitec International, Inc.
    Operator Number
    10033379
    Address
    500 Totten Pond Rd, 10 CityPoint
    City
    Waltham
    State
    MA
    Postal Code
    02451
    Country
    US

    Products

    Device Name Product Code
    Sponge, Ophthalmic HOZ

    Proprietary Names

    Keracel LASIK Corneal Shield Karacel Yavitz Drainage Ring & Flap Cover Visitec Microsurgical Accessory Kit Ophthalmic Surgery Kit Merocel Hardten Cover Keracel LASIK Spear Kit Weck-Cel Sponge Points and Strips Merocel Fluid Collection Bag with Wick Keracel Chayet Drainage Ring Merocel Eye Kit Keracel Yavitz Flap Cover Visitec Eye Fluid Wick Merocel Instrument Wipes Merocel Corneal Light Shield Keracel Cleanfield LASIK Kit Merocel Eye Wick Merocel PVA Eye Spears BVI, Beaver-Visitec International, Weck-cel, Merocel, Keracel Merocel Crystal Anesthesia Ring Merocel Sponge Points Weck-Cel Sponge Points Merocel Cataract Kit Keracel LASIK PVA Eye Spears Merocel Instrument Wipe Kit Weck-Cel Cellulose Eye Spear

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device