Taiwan FDA registration 1910001977c86c7a0437c18f54c002b1
“Bausch & Lomb” enVista Hydrophobic Toric Acrylic Intraocular Lens
TW: “博士倫”恩視非球面散光矯正人工水晶體
Registration details
- Analysis ID
- 1910001977c86c7a0437c18f54c002b1
- License Form
- Ministry of Health Medical Device Import No. 028640
- Customs Code
- DHA05602864002
Company information
- Manufacturer
- BAUSCH & LOMB INCORPORATED
- Manufacturer Country
- United States
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
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
- Jul 21, 2016
- Expiry Date
- Jul 21, 2026
About this record
Access comprehensive regulatory information for “Bausch & Lomb” enVista Hydrophobic Toric Acrylic 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 1910001977c86c7a0437c18f54c002b1 and manufactured by BAUSCH & LOMB INCORPORATED. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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