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Bioteq™ Ureteral Stent Set (Close-Close + With Coating + Without Suture) Series - FDA Registration MDR-03750D

Access comprehensive regulatory information for Bioteq™ Ureteral Stent Set (Close-Close + With Coating + Without Suture) Series in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-03750D 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 - 1-Lan Factory 11 - 1-Lan Taiwan in Taiwan. The device was registered on June 07, 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.

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Taiwan
MDR-03750D
Bioteq™ Ureteral Stent Set (Close-Close + With Coating + Without Suture) Series
Registered medical device in Philippines
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Device Information
Product Name
Bioteq™ Ureteral Stent Set (Close-Close + With Coating + Without Suture) Series
Registration Number
MDR-03750D
Importer & Distribution
Registration Dates
Issuance Date
June 07, 2023
Expiry Date
October 26, 2026