BEUDAMED
    FDA Registration Active 🇮🇳 India

    Quikfuge

    Reg #: 3012315023 · FEI: 3012315023 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    8
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Remi Elektrotechnik Ltd.
    Registration Number
    3012315023
    FEI Number
    3012315023
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Bldg B, Survey No. 65/1, Village - Valiv, Vasai (East)
    City
    Dist. Palghar Maharashtra
    Country
    IN

    Owner / Operator

    Firm Name
    Remi Elektrotechnik Ltd.
    Operator Number
    10050790
    Address
    Remi House, 11 Cama Industrial Estate, Walbhat Road,Goregaon (East)
    City
    Mumbai
    State
    IN-NOTA
    Postal Code
    400 063
    Country
    IN

    US Agent

    Business Name
    mdi Consultants, inc.
    Contact Name
    Alan Schwartz
    Address
    55 Northern Blvd Ste 200
    City
    Great Neck
    State
    NY
    ZIP
    11021
    Country
    US
    Email
    [email protected]
    Phone
    516 4829001

    Products

    Device Name Product Code
    Centrifuge, Blood-Bank For In Vitro Diagnostic Use KSO

    Proprietary Names

    Quikfuge Blood Bank centrifuge KBM 70, KBM 70 Plus, KBM 80 Plus, KBM 90 Plus PRP Centrifuge: PRP-41 Plus, PRP Ultra CENTRIFUGE, BLOOD-BANK FOR IN VITRO DIAGNOSTIC USE: KBM 80i Plus, KBM 90i Plus, CENTRIFUGE, BLOOD-BANK FOR IN VITRO DIAGNOSTIC USE: KBM 80 Plus LCD, KBM 80 Plus TFT PRP Plus Neya 6 Plus, NEYA 18, Neya-24, Neya-36, HCM 6, HCM 15, HCR 16 Plus, HCP 7, HCP 20 HCP 7C, HCP 20C, Neya 18R, Neya 24R, Neya 36R

    Establishment Types

    Manufacture Medical Device