Taiwan FDA registration 25fb4ec72bcdef620fb37ca67c449510

"Steri" introduction/drainage catheter and its accessories (unsterilized)

TW: "史泰瑞" 導入/引流導管及其附件 (未滅菌)

Taiwan·Risk Class 1·UNITED STATES ENDOSCOPY GROUP, INC.;; STERIS Corporation·Registered Aug 09, 2017 – Aug 09, 2027Active

Registration details

Analysis ID: 25fb4ec72bcdef620fb37ca67c449510
Customs Code: DHA09401816400

Company information

Manufacturer: UNITED STATES ENDOSCOPY GROUP, INC.;; STERIS Corporation
Manufacturer Country: United States
Authorized Representative: Sterry Taiwan Corporation

Product details

Intended Use: Limited to the first level of identification scope of the Measures for the Classification and Grading of Medical Devices "Introduction/Drainage Catheters and Their Accessories (I.4200)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4200 Incoming/Drainage Tubes 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 "Steri" introduction/drainage catheter and its 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 25fb4ec72bcdef620fb37ca67c449510 and manufactured by UNITED STATES ENDOSCOPY GROUP, INC.;; STERIS Corporation. The authorized representative in Taiwan is Sterry Taiwan Corporation.

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