Taiwan FDA registration 101496866c2619e66cd6f3c5bda7f194
LENTIS Comfort Toric Intraocular Lens
TW: “藍提視”康福視散光多焦點人工水晶體
Taiwan·Risk Class 3·MD·Teleon Surgical B.V.·Registered Jan 30, 2018 – Jan 30, 2028ActiveRegistration details
- Analysis ID
- 101496866c2619e66cd6f3c5bda7f194
- License Form
- Ministry of Health Medical Device Import No. 030719
- Customs Code
- DHA05603071907
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
- Jan 30, 2018
- Expiry Date
- Jan 30, 2028
About this record
Access comprehensive regulatory information for LENTIS Comfort 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 101496866c2619e66cd6f3c5bda7f194 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