"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.).
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
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
ๆชๅฑๅปถ่้พๆ่

