Taiwan FDA registration a0853f1352fc86de62c56737ef58e79a
“LENTIS” Mplus Toric Intraocular Lens
TW: “藍提視”安普視散光多焦點人工水晶體
Taiwan·Risk Class 3·MD·Teleon Surgical B.V.·Registered Jul 31, 2018 – Jul 31, 2028ActiveRegistration details
- Analysis ID
- a0853f1352fc86de62c56737ef58e79a
- License Form
- Ministry of Health Medical Device Import No. 031228
- Customs Code
- DHA05603122806
Company information
- Manufacturer
- Teleon Surgical B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- UNITED MEDICAL 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
- Jul 31, 2018
- Expiry Date
- Jul 31, 2028
About this record
Access comprehensive regulatory information for “LENTIS” Mplus 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 a0853f1352fc86de62c56737ef58e79a and manufactured by Teleon Surgical B.V.. The authorized representative in Taiwan is UNITED MEDICAL 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