Taiwan FDA registration f476dedaec20661cad78dbf283a07861
“Alcon” Legion FMS Packs
TW: “愛爾康”立復明手術耗材包
Registration details
- Analysis ID
- f476dedaec20661cad78dbf283a07861
- License Form
- Ministry of Health Medical Device Import No. 033958
- Customs Code
- DHA05603395801
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)
- M4670 Crystal Emulsifier
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 18, 2020
- Expiry Date
- Sep 18, 2025
About this record
Access comprehensive regulatory information for “Alcon” Legion FMS Packs in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f476dedaec20661cad78dbf283a07861 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.
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