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“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.

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2215cfb4d28c96891dd697726ce054cd
Registration Details
Taiwan FDA Registration: 2215cfb4d28c96891dd697726ce054cd
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Device Details

“LENTIS” Mplus Multifocal Intraocular Lens
TW: “藍提視”安普視多焦點人工水晶體
Risk Class 3
MD

Registration Details

2215cfb4d28c96891dd697726ce054cd

Ministry of Health Medical Device Import No. 030611

DHA05603061100

Company Information

Netherlands

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