Taiwan FDA registration de8f574740a29bd1dd8ba8bb9c506fd2
“Fotona” Dynamis Line Laser System
TW: “富多拿”黛娜美斯雅各多功能雷射系統
Taiwan·Risk Class 2·MD·Fotona d.o.o.·Registered Apr 12, 2016 – Apr 12, 2021ExpiredRegistration details
- Analysis ID
- de8f574740a29bd1dd8ba8bb9c506fd2
- License Form
- Ministry of Health Medical Device Import No. 028367
- Customs Code
- DHA05602836700
Company information
- Manufacturer
- Fotona d.o.o.
- Manufacturer Country
- Slovenia
- Authorized Representative
- DYNAMIC MEDICAL TECHNOLOGIES INC.
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
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 12, 2016
- Expiry Date
- Apr 12, 2021
About this record
Access comprehensive regulatory information for “Fotona” Dynamis Line 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 de8f574740a29bd1dd8ba8bb9c506fd2 and manufactured by Fotona d.o.o.. 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 DatabasePowered by Pure Global AI89,000+ Devices