Taiwan FDA registration f4a1cc57a37d6d257553b4c9f4e01049

"Sterry" endoscope attachment (unsterilized)

TW: "史泰瑞"內視鏡附件(未滅菌)

Taiwan·Risk Class 1·UNITED STATES ENDOSCOPY GROUP, INC.;; STERIS Corporation·Registered Mar 09, 2018 – Mar 09, 2028Active

Registration details

Analysis ID: f4a1cc57a37d6d257553b4c9f4e01049
Customs Code: DHA09401888701

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 recognition range of the "endoscope and its accessories (H.1500)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.1500 Internal Scope and its accessories
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Mar 09, 2018
Expiry Date: Mar 09, 2028

About this record

Access comprehensive regulatory information for "Sterry" endoscope attachment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f4a1cc57a37d6d257553b4c9f4e01049 and manufactured by UNITED STATES ENDOSCOPY GROUP, INC.;; STERIS Corporation. The authorized representative in Taiwan is Sterry Taiwan Corporation.

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