Pure Global

"Schneihui" manual arthroscopic equipment (sterilization) - Taiwan Registration 3f59cffaea060b180dc467dcaf4aa6f5

Access comprehensive regulatory information for "Schneihui" manual arthroscopic equipment (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3f59cffaea060b180dc467dcaf4aa6f5 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
3f59cffaea060b180dc467dcaf4aa6f5
Registration Details
Taiwan FDA Registration: 3f59cffaea060b180dc467dcaf4aa6f5
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Schneihui" manual arthroscopic equipment (sterilization)
TW: โ€œๅฒ่€่ผโ€ๆ‰‹ๅ‹•ๅผ้—œ็ฏ€้กๅ™จๆ (ๆป…่Œ)
Risk Class 1

Registration Details

3f59cffaea060b180dc467dcaf4aa6f5

DHA04400775503

Company Information

Product Details

Limited to the first level identification range of the classification and grading management method for medical equipment "Arthroscopy (N.1100)".

N Orthopedics

N.1100 Closing Lenses

Input;; QMS/QSD

Dates and Status

May 22, 2009

May 22, 2029