Taiwan FDA registration c5a4fe9c340ef087a5c8904bba26f65f
“Valeant Med” FOCUSFORCE RE-VISION Multifocal Intraocular Lens
TW: “威朗”博科視多焦點人工水晶體
Taiwan·Risk Class 3·MD·VALEANT MED Sp. z o.o.·Registered Oct 02, 2017 – Oct 02, 2022ExpiredRegistration details
- Analysis ID
- c5a4fe9c340ef087a5c8904bba26f65f
- License Form
- Ministry of Health Medical Device Import No. 030268
- Customs Code
- DHA05603026800
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
- Oct 02, 2017
- Expiry Date
- Oct 02, 2022
About this record
Access comprehensive regulatory information for “Valeant Med” FOCUSFORCE RE-VISION Multifocal 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 c5a4fe9c340ef087a5c8904bba26f65f 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