Taiwan FDA registration bb534a92738341376df96f80916f5e9d
“LENTIS” HydroSmart Posterior Chamber Intraocular Lens with Multifocal Toric Optic
TW: "藍提視”多焦點散光人工水晶體
Taiwan·Risk Class 3·MD·Teleon Surgical B.V.·Registered Aug 22, 2014 – Aug 22, 2024ExpiredRegistration details
- Analysis ID
- bb534a92738341376df96f80916f5e9d
- License Form
- Ministry of Health Medical Device Import No. 026200
- Customs Code
- DHA05602620003
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
- Aug 22, 2014
- Expiry Date
- Aug 22, 2024
About this record
Access comprehensive regulatory information for “LENTIS” HydroSmart Posterior Chamber Intraocular Lens with Multifocal Toric Optic in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number bb534a92738341376df96f80916f5e9d and manufactured by Teleon Surgical B.V.. The authorized representative in Taiwan is UNITED MEDICAL INC..
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