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Endure Disposable Vacuum Blood Collection Tube-Glass Type: EDTA K2 - FDA Registration MDR-050151

Access comprehensive regulatory information for Endure Disposable Vacuum Blood Collection Tube-Glass Type: EDTA K2 in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-050151 and manufactured by Zhejiang Gongdong Medical Technology Co., Ltd. No. 10, Beiyuan Ave., Huangyan, Taizhou, Zhejiang, China in China. The device was registered on May 30, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Endure Medical, Inc.), 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-050151
Endure Disposable Vacuum Blood Collection Tube-Glass Type: EDTA K2
Registered medical device in Philippines
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Device Information
Product Name
Endure Disposable Vacuum Blood Collection Tube-Glass Type: EDTA K2
Registration Number
MDR-050151
Importer & Distribution
Importer/Distributor
Endure Medical, Inc.
Registration Dates
Issuance Date
May 30, 2024
Expiry Date
January 09, 2028