GLAB Vacuum Collection Blood Tube EDTA K3 (PET) - FDA Registration IVDR-00885B

Access comprehensive regulatory information for GLAB Vacuum Collection Blood Tube EDTA K3 (PET) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00885B and manufactured by Ningbo Sintrue Medical Instruments Co., Ltd. - Room 11-1-1, Building 8, No.2 Zhuyi Road, Hi Tech Zone, Ningbo City, Zheijian 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 September 19, 2024.

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.