BEUDAMED
    FDA Registration Active 🇫🇷 France

    AESCULAP SAS

    Reg #: 9681258 · FEI: 3001354499 · Expires 2026
    View on FDA
    Products
    3
    Proprietary Names
    2
    Establishment Types
    2
    Classifications
    3

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    Registration Details

    Registration Name
    AESCULAP SAS
    Registration Number
    9681258
    FEI Number
    3001354499
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    BOULEVARD DU MARECHAL JUIN, BP 2024
    City
    CHAUMONT Grand Est
    Country
    FR

    Owner / Operator

    Firm Name
    Aesculap AG
    Operator Number
    8010193
    Address
    Am Aesculap-Platz
    City
    Tuttlingen
    State
    Baden-Wurttemberg
    Postal Code
    78532
    Country
    DE
    Correspondent
    Kamaal Anas

    US Agent

    Business Name
    Aesculap, Inc.
    Contact Name
    Kamaal Anas
    Address
    3773 Corporate Parkway
    City
    Center Valley
    State
    PA
    ZIP
    18034
    Country
    US
    Email
    [email protected]
    Phone
    610 9849071 ext. 5071

    Products

    Device Name Product Code
    Impactor HWA
    Orthopedic Manual Surgical Instrument LXH
    Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer JWH

    Proprietary Names

    AESCULAP Aesculap

    Establishment Types

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