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

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-05860C and manufactured by Bioteque Corporation 5F-6, No. 23 , Sec. 1, Chang-An E. Road, Taipei 104, Taiwan, R.O.C in Taiwan. The device was registered on November 15, 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.