BIOTEQ® Hemodialysis Catheter Kit - FDA Registration MDR-05860 B

Access comprehensive regulatory information for BIOTEQ® Hemodialysis Catheter Kit in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05860 B and manufactured by Bioteque Corporation - 5F-6, No. 23, Sec. 1, Chang-An E. Road, Taipei 104, Taiwan, R.O.C. Mfd by: Bioteque Corporation I-Lan Factory II - Ilan, Taiwan in Taiwan. The device was registered on August 14, 2023.

This page provides complete registration details including manufacturer information, importer/distributor details (Bonteq Medical Distribution Phil. 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.