BEUDAMED
    FDA Registration Active 🇨🇳 China

    TRANSFER DEVICE(Model: KDB-506A,KDB-506B,KDB-506C,KDB-506E,KDB-506F,KDB-506series,KDB-507,KDB-507A,KDB-507B)

    Reg #: 3030222359 · FEI: 3030222359 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    ZHONGSHAN KANGDEBAO (KDB) REHABILITATION EQUIPMENT CO., LTD
    Registration Number
    3030222359
    FEI Number
    3030222359
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    One of the 1st floor, No. 24, Longcheng Road, Shenglong Village, Xiaolan Town
    City
    Zhongshan Guangdong
    Country
    CN

    Owner / Operator

    Firm Name
    Zhongshan Kangdebao (KDB) Rehabilitation Equipment Co., Ltd
    Operator Number
    10089229
    Address
    One of the 1st floor, No. 24, Longcheng Road, Shenglong Village, Xiaolan Town
    City
    Zhongshan
    State
    Guangdong
    Postal Code
    528414
    Country
    CN
    Correspondent
    Weijian Lin

    US Agent

    Business Name
    SPICA MEDTECH CORP
    Contact Name
    Creekon Yang
    Address
    1020 LINCOLN ST
    City
    Denver
    State
    CO
    ZIP
    80203
    Country
    US
    Email
    [email protected]
    Phone
    720 6176666

    Products

    Device Name Product Code
    Device, Transfer, Patient, Manual FMR

    Proprietary Names

    TRANSFER DEVICE(Model: KDB-506A,KDB-506B,KDB-506C,KDB-506E,KDB-506F,KDB-506series,KDB-507,KDB-507A,KDB-507B) TRANSFER DEVICE(Model: KDB-505, KDB-505A, KDB-505B, KDB-505C, KDB-505D,KDB-505E,KDB-505F, KDB-505series,KDB-506) TRANSFER DEVICE(Model: KDB-507C, KDB-507series, KDB-508, KDB-508A,KDB-508B, KDB-508C, KDB-508series,KDB-509series)

    Establishment Types

    Manufacture Medical Device