"Sterry" miniature biosensory forceps
Taiwan·Risk Class 2·STERIS CORPORATION;; UNITED STATES ENDOSCOPY GROUP, INC.·Registered Apr 16, 2021 – Apr 16, 2026Expired- Analysis ID
- 55d3e210524a130cd9ddd31c7714736f
- Customs Code
- DHA05603443401
- Manufacturer Country
- United States
- Authorized Representative
- Sterry Taiwan Corporation
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1075 腸胃科-泌尿科生檢器械
- Import Information
- import
- Registration Date
- Apr 16, 2021
- Expiry Date
- Apr 16, 2026
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Access comprehensive regulatory information for "Sterry" miniature biosensory forceps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 55d3e210524a130cd9ddd31c7714736f and manufactured by STERIS CORPORATION;; UNITED STATES ENDOSCOPY GROUP, INC.. The authorized representative in Taiwan is Sterry Taiwan Corporation.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including STERIS CORPORATION;; UNITED STATES ENDOSCOPY GROUP, INC., and 1 recent registrations in the same category. 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.