BEUDAMED
    FDA Registration Active 🇫🇷 France

    LIGAFIX ratchet screwdriver rod Diameter 7-8 mm, Catalog Number LIG9000310

    Reg #: 3004549189 · FEI: 3004051158 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    11
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    SCIENCE & BIO MATERIALS, S.B.M. SAS
    Registration Number
    3004549189
    FEI Number
    3004051158
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    ZI DU MONGE
    City
    LOURDES Hautes-Pyrenees
    Country
    FR

    Owner / Operator

    Firm Name
    SCIENCE & BIO MATERIALS
    Operator Number
    9063735
    Address
    S.B.M. SAS - ZI DU MONGE, --
    City
    Lourdes
    State
    Hautes-Pyrenees
    Postal Code
    65100
    Country
    FR
    Correspondent
    Anne - COSPIN

    US Agent

    Business Name
    Dawa Medical LLC
    Contact Name
    Stephan Toupin
    Address
    7320 NW 12th Street, Suite 103
    City
    Miami
    State
    FL
    ZIP
    33126
    Country
    US
    Email
    [email protected]
    Phone
    786 7311159

    Products

    Device Name Product Code
    Screwdriver HXX

    Proprietary Names

    LIGAFIX ratchet screwdriver rod Diameter 7-8 mm, Catalog Number LIG9000310 LIGAFIX ratchet screwdriver rod Diameter 9-10-11 mm, Catalog Number LIG9000311 ComposiTCP™ Modular Driver, Catalog Number 110004607 LIGAFIX blue screwdriver for 9, 10 & 11 mm screws, Catalog Number LIG9009017 LIGAFIX green screwdriver for 7 & 8 mm screws, Catalog Number LIG9008046 FIXIT Knotless / ecoFIX Knotless Screwdriver, Catalog Number EPA9000315 ecoFIX diameter 4.5 mm Screwdriver, Catalog Number EPA9000401 ComposiTCP™ Modular Driver, Catalog Number 905274 Screwdriver for OTIS screw extraction, Catalog Number EVO9069439 OTIS-C-PLUS diam. 3.5 mm hexagonal screwdriver, Catalog Number EVO9069436 ecoFIX diameter 5.5-6.5 mm Screwdriver, Catalog Number EPA9000403

    Establishment Types

    Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198