“Gyrus ACMI” Tecoflex Quadra-Coil Multi-Length Ureteral Stents - Taiwan Registration 0b94f1da941d9f5eb2ba968d1383fafd
Access comprehensive regulatory information for “Gyrus ACMI” Tecoflex Quadra-Coil Multi-Length Ureteral Stents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0b94f1da941d9f5eb2ba968d1383fafd and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Registration Details
0b94f1da941d9f5eb2ba968d1383fafd
Ministry of Health Medical Device Import No. 028050
DHA05602805007
Product Details
For details, it is Chinese approved copy of the imitation order
H Gastroenterology-urology devices
H4620 Ureteral stents
Imported from abroad
Dates and Status
Jan 15, 2016
Jan 15, 2026

