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“Hanita”Intensity Intraocular Lens - Taiwan Registration d27218c3f4ff2a6c038c70512c8a98ce

Access comprehensive regulatory information for “Hanita”Intensity 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 d27218c3f4ff2a6c038c70512c8a98ce 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.

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d27218c3f4ff2a6c038c70512c8a98ce
Registration Details
Taiwan FDA Registration: d27218c3f4ff2a6c038c70512c8a98ce
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Device Details

“Hanita”Intensity Intraocular Lens
TW: “漢寧達”易視能人工水晶體
Risk Class 3
MD

Registration Details

d27218c3f4ff2a6c038c70512c8a98ce

Ministry of Health Medical Device Import No. 036052

DHA05603605207

Company Information

Israel

Product Details

Details are as detailed as approved Chinese instructions

M Ophthalmology

M3600 intraocular lens

Imported from abroad

Dates and Status

Nov 21, 2022

Nov 21, 2027