Taiwan FDA registration d533ae297d03c971fafc6fc005fc3ee2

"Schnee-Fai" hysteroscopy and its accessories (sterilization)

TW: "史耐輝"子宮鏡及其附件(滅菌)

Taiwan·Risk Class 1·SMITH & NEPHEW, INC. ENDOSCOPY DIVISION·Registered Dec 23, 2015 – Dec 23, 2020Cancelled

Registration details

Analysis ID: d533ae297d03c971fafc6fc005fc3ee2
Customs Code: DHA09401600901

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 identification range of the Measures for the Administration of Medical Devices "Hysteroscopy and its Accessories (L.1690)".
Product Type (Level 1): l Obstetrics and Gynecology
Product Type (Level 2): L.1690 Uterine mirrors and their accessories
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Dec 23, 2015
Expiry Date: Dec 23, 2020
Cancellation Date: Jul 15, 2022

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Schnee-Fai" hysteroscopy and its 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 d533ae297d03c971fafc6fc005fc3ee2 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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