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“Hanita” SeeLens AF Aspheric Hydrophilic Intraocular Lens - Taiwan Registration 6b7056744e61da16beaca6d3e4f4a19e

Access comprehensive regulatory information for “Hanita” SeeLens AF Aspheric Hydrophilic 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 6b7056744e61da16beaca6d3e4f4a19e and manufactured by HANITA LENSES. The authorized representative in Taiwan is OCU-MED INC..

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6b7056744e61da16beaca6d3e4f4a19e
Registration Details
Taiwan FDA Registration: 6b7056744e61da16beaca6d3e4f4a19e
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Device Details

“Hanita” SeeLens AF Aspheric Hydrophilic Intraocular Lens
TW: “漢寧達”愛視能非球面人工水晶體
Risk Class 3
MD

Registration Details

6b7056744e61da16beaca6d3e4f4a19e

Ministry of Health Medical Device Import No. 027248

DHA05602724800

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 01, 2015

Apr 01, 2025