BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    ARCERA GMBH

    Reg #: 3015373820 · FEI: 3015373820 · Expires 2026
    View on FDA
    Products
    3
    Proprietary Names
    0
    Establishment Types
    1
    Classifications
    3

    Registration Details

    Registration Name
    ARCERA GMBH
    Registration Number
    3015373820
    FEI Number
    3015373820
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    Levelingstrasse 8
    City
    Munich Bavaria
    Country
    DE

    Regulatory Submissions

    PMA Number
    P140029

    Owner / Operator

    Firm Name
    Arcera GmbH
    Operator Number
    10060255
    Address
    Levelingstrasse 8
    City
    Munich
    State
    Bavaria
    Postal Code
    81673
    Country
    DE
    Correspondent
    Franz-Josef Wienhold

    Products

    Device Name Product Code
    Implant, Dermal, For Aesthetic Use LMH
    Acid, Hyaluronic, Intraarticular MOZ
    Implant, Dermal, For Aesthetic Use In The Hands PKY

    Establishment Types

    Repack or Relabel Medical Device