Taiwan FDA registration 50c85a5002105d795a7eef8bad25cfa3
“Quanta” Fiber Dust Laser System and Accessories
TW: “貫達碩”銩光雷射系統及其配件
Taiwan·Risk Class 2·MD·Quanta System S.p.A·Registered Jun 15, 2022 – Jun 15, 2027ActiveRegistration details
- Analysis ID
- 50c85a5002105d795a7eef8bad25cfa3
- License Form
- Ministry of Health Medical Device Import No. 035582
- Customs Code
- DHA05603558205
Company information
- Manufacturer
- Quanta System S.p.A
- Manufacturer Country
- Italy
- Authorized Representative
- KUAN FWA MED CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 15, 2022
- Expiry Date
- Jun 15, 2027
About this record
Access comprehensive regulatory information for “Quanta” Fiber Dust Laser System and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 50c85a5002105d795a7eef8bad25cfa3 and manufactured by Quanta System S.p.A. The authorized representative in Taiwan is KUAN FWA MED 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