"Stryker" lumbar fusion device - Taiwan Registration e270cbd02375f2f7b6d31fe5f09ee826
Access comprehensive regulatory information for "Stryker" lumbar 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 e270cbd02375f2f7b6d31fe5f09ee826 and manufactured by STRYKER SPINE SAS. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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
e270cbd02375f2f7b6d31fe5f09ee826
Registration Details
Taiwan FDA Registration: e270cbd02375f2f7b6d31fe5f09ee826
Device Details
"Stryker" lumbar fusion device
TW: โๅฒ่ณฝๅ
โ่
ฐๆค้่ๅๅจ
Risk Class 2

