“LENTIS” Mplus Multifocal Intraocular Lens - Taiwan Registration 2215cfb4d28c96891dd697726ce054cd
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..
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.
Device Details
Registration Details
2215cfb4d28c96891dd697726ce054cd
Ministry of Health Medical Device Import No. 030611
DHA05603061100
Product Details
For details, it is Chinese approved copy of the imitation order
M Ophthalmic devices
M3600 intraocular lens
Imported from abroad
Dates and Status
Dec 11, 2017
Dec 11, 2027

