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Golden Vac Disposable Vacuum Blood Collection Tube (EDTA K2) - FDA Registration MDR-06698

Access comprehensive regulatory information for Golden Vac Disposable Vacuum Blood Collection Tube (EDTA K2) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-06698 and manufactured by Zhejiang Gongdong Medical Technology Co., Ltd. - No. 10 Beiyuan Ave., Huangyan 318020 Taizhou, Zhejiang Peopleโ€™s Republic of China in CHINA. The device was registered on August 07, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Rezostar Corporation), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.

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CHINA
MDR-06698
Golden Vac Disposable Vacuum Blood Collection Tube (EDTA K2)
Registered medical device in Philippines
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Device Information
Product Name
Golden Vac Disposable Vacuum Blood Collection Tube (EDTA K2)
Registration Number
MDR-06698
Importer & Distribution
Importer/Distributor
Rezostar Corporation
Registration Dates
Issuance Date
August 07, 2024
Expiry Date
April 24, 2029