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"Schnee-Fai" hysteroscopy and its accessories (sterilization) - Taiwan Registration d533ae297d03c971fafc6fc005fc3ee2

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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d533ae297d03c971fafc6fc005fc3ee2
Registration Details
Taiwan FDA Registration: d533ae297d03c971fafc6fc005fc3ee2
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Device Details

"Schnee-Fai" hysteroscopy and its accessories (sterilization)
TW: "ๅฒ่€่ผ"ๅญๅฎฎ้กๅŠๅ…ถ้™„ไปถ(ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

d533ae297d03c971fafc6fc005fc3ee2

DHA09401600901

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Hysteroscopy and its Accessories (L.1690)".

l Obstetrics and Gynecology

L.1690 Uterine mirrors and their accessories

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Dec 23, 2015

Dec 23, 2020

Jul 15, 2022

Cancellation Information

Logged out

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