Pure Global

"Chang'an" cervical intervertebral fusion device - Taiwan Registration 10c55463691c56aef8f50dbf90a95d3d

Access comprehensive regulatory information for "Chang'an" cervical intervertebral fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 10c55463691c56aef8f50dbf90a95d3d and manufactured by WELLONG INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is WELLONG INSTRUMENTS CO., LTD..

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
10c55463691c56aef8f50dbf90a95d3d
Registration Details
Taiwan FDA Registration: 10c55463691c56aef8f50dbf90a95d3d
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Chang'an" cervical intervertebral fusion device
TW: โ€œ้•ทๅฎ‰โ€้ ธๆคŽๆคŽ้–“่žๅˆๅ™จ
Risk Class 2

Registration Details

10c55463691c56aef8f50dbf90a95d3d

DHY00500245405

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedics

N.3060 ๆคŽ้ซ”้–“ไน‹่„ŠๆคŽ็Ÿฏๆญฃๅ›บๅฎš็‰ฉ

Domestic

Dates and Status

Jun 24, 2008

Jun 24, 2028