Taiwan FDA registration 4478d2b338f8184016300617ac15c4d3
“LightMed” LightLas Pattern Scanning System
TW: “承賢”掃描式雷射治療儀
Taiwan·Risk Class 2·MD·LIGHTMED CORPORATION·Registered Jan 13, 2016 – Jan 13, 2026ExpiredRegistration details
- Analysis ID
- 4478d2b338f8184016300617ac15c4d3
- License Form
- Ministry of Health Medical Device Manufacturing No. 005298
Company information
- Manufacturer
- LIGHTMED CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LIGHTMED CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M4390 Ophthalmic laser unit
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jan 13, 2016
- Expiry Date
- Jan 13, 2026
About this record
Access comprehensive regulatory information for “LightMed” LightLas Pattern Scanning System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4478d2b338f8184016300617ac15c4d3 and manufactured by LIGHTMED CORPORATION. The authorized representative in Taiwan is LIGHTMED CORPORATION.
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