GLAB Vacuum Collection Blood Tube with EDTA K2 (PET) - FDA Registration IVDR-00988 A

Access comprehensive regulatory information for GLAB Vacuum Collection Blood Tube with EDTA K2 (PET) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00988 A and manufactured by Ningbo Sintrue Medical Instruments Co., Ltd.- Room 11-1-1, Building 8, No. 2 Zhuyi Road, Hi Tech Zone, Ningbo City, Zhejiang Province, China Mfd. by: Hebei Xiangyuan Medical Devices Co., Ltd.- North Wufan Road, Xinle City, Hebei Province, China in China. The device was registered on July 10, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Whimgee Enterprises), 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.