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“ROHTO” NEO EYE Aspheric Foldable Lens - Taiwan Registration 58a36d64d42e522d311fbd6b11df08ac

Access comprehensive regulatory information for “ROHTO” NEO EYE Aspheric Foldable Lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 58a36d64d42e522d311fbd6b11df08ac and manufactured by PT Rohto Laboratories Indonesia. The authorized representative in Taiwan is SHIN SHENG PHARMACEUTICAL CO., LTD..

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58a36d64d42e522d311fbd6b11df08ac
Registration Details
Taiwan FDA Registration: 58a36d64d42e522d311fbd6b11df08ac
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Device Details

“ROHTO” NEO EYE Aspheric Foldable Lens
TW: “樂敦”新視非球面人工水晶體
Risk Class 3
MD

Registration Details

58a36d64d42e522d311fbd6b11df08ac

Ministry of Health Medical Device Import No. 025821

DHA05602582104

Company Information

Indonesia

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

Feb 24, 2014

Feb 24, 2024