Taiwan FDA registration 2215cfb4d28c96891dd697726ce054cd
“LENTIS” Mplus Multifocal Intraocular Lens
TW: “藍提視”安普視多焦點人工水晶體
Taiwan·Risk Class 3·MD·Teleon Surgical B.V.·Registered Dec 11, 2017 – Dec 11, 2027ActiveRegistration details
- Analysis ID
- 2215cfb4d28c96891dd697726ce054cd
- License Form
- Ministry of Health Medical Device Import No. 030611
- Customs Code
- DHA05603061100
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
- Dec 11, 2017
- Expiry Date
- Dec 11, 2027
About this record
Access comprehensive regulatory information for “LENTIS” Mplus 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 2215cfb4d28c96891dd697726ce054cd and manufactured by Teleon Surgical B.V.. The authorized representative in Taiwan is UNITED MEDICAL INC..
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