Taiwan FDA registration 19ea1cde5f61c823f283abae144dd752
“VSY” ACRIVA BB TORIC INTRAOCULAR LENS
TW: “惟視艾” 艾卡瑞爾單焦散光人工水晶體
Taiwan·Risk Class 3·MD·VSY Biotechnology GmbH·Registered May 26, 2017 – May 26, 2027ActiveRegistration details
- Analysis ID
- 19ea1cde5f61c823f283abae144dd752
- License Form
- Ministry of Health Medical Device Import No. 029775
- Customs Code
- DHA05602977504
Company information
- Manufacturer
- VSY Biotechnology GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- CLINICO INC.
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)
- M3600 intraocular lens
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 26, 2017
- Expiry Date
- May 26, 2027
About this record
Access comprehensive regulatory information for “VSY” ACRIVA BB TORIC INTRAOCULAR LENS in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 19ea1cde5f61c823f283abae144dd752 and manufactured by VSY Biotechnology GmbH. The authorized representative in Taiwan is CLINICO 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