"Epter" Detrik double-cavity microtubules - Taiwan Registration e99e3812cf8a31aab515d047a6d267ab
Access comprehensive regulatory information for "Epter" Detrik double-cavity microtubules in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e99e3812cf8a31aab515d047a6d267ab and manufactured by APT Medical Inc.. The authorized representative in Taiwan is NO.1 BIOTECHNOLOGY 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
e99e3812cf8a31aab515d047a6d267ab
Registration Details
Taiwan FDA Registration: e99e3812cf8a31aab515d047a6d267ab
Device Details
"Epter" Detrik double-cavity microtubules
TW: โๅๆฎ็นโ ๅพท่ๅ
้่
ๅพฎๅฐ็ฎก
Risk Class 2

