Pure Global

“Hanita” SeeLens MF Aspheric Multifocal Intraocular Lens - Taiwan Registration fa9274173f58b5431fb79f68e6c71344

Access comprehensive regulatory information for “Hanita” SeeLens MF Aspheric 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 fa9274173f58b5431fb79f68e6c71344 and manufactured by HANITA LENSES. The authorized representative in Taiwan is OCU-MED 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 Database
Powered by Pure Global AI
89,000+ Devices
fa9274173f58b5431fb79f68e6c71344
Registration Details
Taiwan FDA Registration: fa9274173f58b5431fb79f68e6c71344
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Hanita” SeeLens MF Aspheric Multifocal Intraocular Lens
TW: “漢寧達”全視能非球面多焦點人工水晶體
Risk Class 3
MD

Registration Details

fa9274173f58b5431fb79f68e6c71344

Ministry of Health Medical Device Import No. 027251

DHA05602725102

Company Information

Israel

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

Apr 02, 2015

Apr 02, 2025