Taiwan FDA registration ccd2b07708259a54db1bb54c9816b787
“Valeant Med” FOCUSforce Aspheric Intraocular Lens
TW: “威朗”博科視非球面人工水晶體
Registration details
- Analysis ID
- ccd2b07708259a54db1bb54c9816b787
- License Form
- Ministry of Health Medical Device Import No. 030009
- Customs Code
- DHA05603000902
Company information
- Manufacturer
- VALEANT MED Sp. z o.o.
- Manufacturer Country
- Poland
- 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
- Aug 11, 2017
- Expiry Date
- Aug 11, 2022
About this record
Access comprehensive regulatory information for “Valeant Med” FOCUSforce Aspheric 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 ccd2b07708259a54db1bb54c9816b787 and manufactured by VALEANT MED Sp. z o.o.. 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