Taiwan FDA registration 20569d888a7b8e6f974f0344c6c19ac5
“Lutronic” enCurve System
TW: “儷妮可”高頻電磁場系統
Taiwan·Risk Class 2·MD·Lutronic Corporation·Registered Sep 04, 2017 – Sep 04, 2022ExpiredRegistration details
- Analysis ID
- 20569d888a7b8e6f974f0344c6c19ac5
- License Form
- Ministry of Health Medical Device Import No. 030205
- Customs Code
- DHA05603020502
Company information
- Manufacturer
- Lutronic Corporation
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- VICTORY EIGHT ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 04, 2017
- Expiry Date
- Sep 04, 2022
About this record
Access comprehensive regulatory information for “Lutronic” enCurve System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 20569d888a7b8e6f974f0344c6c19ac5 and manufactured by Lutronic Corporation. The authorized representative in Taiwan is VICTORY EIGHT ENTERPRISE 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 DatabasePowered by Pure Global AI89,000+ Devices