Taiwan FDA registration 279ecb6b0e0153d3af138847de164fbd

"Schneihui" endoscope accessories (sterile/unsterilized)

TW: "史耐輝" 內視鏡附件 (滅菌/未滅菌)

Taiwan·Risk Class 1·SMITH & NEPHEW, INC. ENDOSCOPY DIVISION·Registered Jul 19, 2017 – Jul 19, 2022Cancelled

Registration details

Analysis ID: 279ecb6b0e0153d3af138847de164fbd
Customs Code: DHA09401808603

Company information

Manufacturer: SMITH & NEPHEW, INC. ENDOSCOPY DIVISION
Manufacturer Country: United States
Authorized Representative: SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.)

Product details

Intended Use: Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Endoscopes and Their Accessories (H.1500)".
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: Jul 19, 2017
Expiry Date: Jul 19, 2022
Cancellation Date: Apr 12, 2024

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Schneihui" endoscope accessories (sterile/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 279ecb6b0e0153d3af138847de164fbd and manufactured by SMITH & NEPHEW, INC. ENDOSCOPY DIVISION. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).

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