Taiwan FDA registration ee5cd2eaaec051cc8d83a989e180c1b2
“Alcon” LenSx Laser Patient Interface
TW: “愛爾康” 雷視能雷射患者介面
Registration details
- Analysis ID
- ee5cd2eaaec051cc8d83a989e180c1b2
- License Form
- Ministry of Health Medical Device Import No. 030784
- Customs Code
- DHA05603078405
Company information
- Manufacturer
- Alcon Research, LLC
- Manufacturer Country
- United States
- Authorized Representative
- ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND)
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
- Imported from abroad
Dates and status
- Registration Date
- Mar 27, 2018
- Expiry Date
- Mar 27, 2028
About this record
Access comprehensive regulatory information for “Alcon” LenSx Laser Patient Interface in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ee5cd2eaaec051cc8d83a989e180c1b2 and manufactured by Alcon Research, LLC. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).
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