Taiwan FDA registration 38ef89c2d9f28d32ce97ad76a81764a8

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

TW: "史泰瑞" 手動式胃腸科-泌尿科手術器械及其附件 (滅菌)
Taiwan flagTaiwan·Risk Class 1·UNITED STATES ENDOSCOPY GROUP, INC.;; STERIS Corporation·Registered Mar 05, 2018 – Mar 05, 2028Active
Registration details
Analysis ID
38ef89c2d9f28d32ce97ad76a81764a8
Customs Code
DHA09401885600
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
Mar 05, 2018
Expiry Date
Mar 05, 2028
About this record

Access comprehensive regulatory information for "Sterry" Manual Gastroenterology-Urology Surgical Instruments and Their Accessories (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 38ef89c2d9f28d32ce97ad76a81764a8 and manufactured by UNITED STATES ENDOSCOPY GROUP, INC.;; STERIS Corporation. The authorized representative in Taiwan is Sterry Taiwan Corporation.

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.

Free DatabasePowered by Pure Global AI89,000+ Devices