BEUDAMED
    FDA Registration Active 🇨🇳 China

    Capilary blood collection tube with sodium fluoride/potassium oxalate

    Reg #: 3005739529 · FEI: 3005739529 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    7
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Zhejiang Gongdong Medical Technology Co., Ltd
    Registration Number
    3005739529
    FEI Number
    3005739529
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    a)No 10 & 39 ,Beiyuan Ave., b)No.88 Jingxian Rd. Huangyan
    City
    TAIZHOU Zhejiang
    Country
    CN

    Owner / Operator

    Firm Name
    ZHEJIANG GONGDONG MEDICAL TECHNOLOGY CO., LTD.
    Operator Number
    9072045
    Address
    BEICHENG INDUSTRIAL AREA, HUANGYAN
    City
    TAIZHOU
    State
    Zhejiang
    Postal Code
    318020
    Country
    CN
    Correspondent
    Rongqing - Dai

    Products

    Device Name Product Code
    Tube, Collection, Capillary Blood GIO

    Proprietary Names

    Capilary blood collection tube with sodium fluoride/potassium oxalate Capilary Blood Collection Tubes 9NC Coagulation Sodium Citrate 3.2%; Capilary blood collection tube with EDTAK3;Capilary blood collection tube with Lithium heparin; Capilary blood collection tube with Sodium heparin;Capilary blood collection tube with sodium fluoride/sodium heparin; Capilary blood collection tube with clot activator and Gel;Capilary blood collection tube with EDTAK2; Capilary blood collection tube with clot activator;Capilary blood collection tube no activator; Capilary Blood Collection Tubes 9NC Coagulation Sodium Citrate 3.8%

    Establishment Types

    Manufacture Medical Device