Bioteq® Guidewire, PTFE Coated - FDA Registration MDR-04015A

Access comprehensive regulatory information for Bioteq® Guidewire, PTFE Coated in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-04015A and manufactured by Bioteque Corp. 5F-6, No. 23, Sec. 1, Chang-An E. Road, Taipei 104, Taiwan Mfd by: Bioteque Corporation I-Lan Factory II - No. 5, Chung Cheng Road, Su-Ao Cheng, I-Lan, Taiwan in Taiwan. The device was registered on June 11, 2024.

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.