"Kentila" diode laser system - Taiwan Registration 695047b1588ea60de3edc0261ab0b636
Access comprehensive regulatory information for "Kentila" diode laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 695047b1588ea60de3edc0261ab0b636 and manufactured by CANDELA CORPORATION. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
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
695047b1588ea60de3edc0261ab0b636
Registration Details
Taiwan FDA Registration: 695047b1588ea60de3edc0261ab0b636
Device Details
"Kentila" diode laser system
TW: "่ฏ็ฌฌๆ" ไบๆฅต้ซ้ทๅฐ็ณป็ตฑ
Risk Class 2
Cancelled

