“Gyrus ACMI” Silicone Double-J, Tractfinder, and Classic Closed Tip Ureteral Stents - Taiwan Registration 483008e9eaa5623ab376f64064d8ce67
Access comprehensive regulatory information for “Gyrus ACMI” Silicone Double-J, Tractfinder, and Classic Closed Tip 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 483008e9eaa5623ab376f64064d8ce67 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
483008e9eaa5623ab376f64064d8ce67
Ministry of Health Medical Device Import No. 027385
DHA05602738507
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
May 12, 2015
May 12, 2025

