Taiwan FDA registration 245cc77e58bf4e17e46ffad259dca0b1

"Sterry" Manual Gastroenterology-Urology Surgical Instruments and Their Accessories (Unsterilized)

TW: "史泰瑞" 手動式胃腸科-泌尿科手術器械及其附件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·UNITED STATES ENDOSCOPY GROUP, INC.;; STERIS Corporation·Registered Aug 09, 2017 – Aug 09, 2027Active
Registration details
Analysis ID
245cc77e58bf4e17e46ffad259dca0b1
Customs Code
DHA09401816308
Company information
Manufacturer Country
United States
Authorized Representative
Sterry Taiwan Corporation
Product details
Intended Use
Limited to the first level identification scope of the classification and grading management method for medical equipment "Manual Gastroenterology-Urology Surgical Instruments and Their Accessories (H.4730)".
Product Type (Level 1)
H Gastroenterology and urology
Product Type (Level 2)
H.4730 H.4730 Hand Gastroentero-Urology Surgical Instruments and Accessories
Import Information
import
Dates and status
Registration Date
Aug 09, 2017
Expiry Date
Aug 09, 2027
About this record

Access comprehensive regulatory information for "Sterry" Manual Gastroenterology-Urology Surgical Instruments and Their Accessories (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 245cc77e58bf4e17e46ffad259dca0b1 and manufactured by UNITED STATES ENDOSCOPY GROUP, INC.;; STERIS Corporation. The authorized representative in Taiwan is Sterry Taiwan Corporation.

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