"Schneihui" articular cartilage probe - Taiwan Registration 4aceac736e584d6b935fc97207696169
Access comprehensive regulatory information for "Schneihui" articular cartilage probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4aceac736e584d6b935fc97207696169 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
For details, it is Chinese approved copy of the imitation order.
I General, Plastic Surgery and Dermatology
import
Dates and Status
Mar 04, 2008
Mar 04, 2018
Nov 15, 2019
Cancellation Information
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