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Diken Vision Multi-Action Maintenance Solution - Taiwan Registration 5579f9b622af027bdd014d7b5d899575

Access comprehensive regulatory information for Diken Vision Multi-Action Maintenance Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5579f9b622af027bdd014d7b5d899575 and manufactured by NANG KUANG PHARMACEUTICAL CO., LTD.. The authorized representative in Taiwan is NANG KUANG PHARMACEUTICAL CO., LTD..

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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5579f9b622af027bdd014d7b5d899575
Registration Details
Taiwan FDA Registration: 5579f9b622af027bdd014d7b5d899575
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Device Details

Diken Vision Multi-Action Maintenance Solution
TW: ๅธๅบท่ฆ–ๆฝคๅคšๆ•ˆไฟ้คŠๆถฒ
Risk Class 2

Registration Details

5579f9b622af027bdd014d7b5d899575

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmology

M.5928 Products for the preservation of soft contact lenses;; M.5918 Rigid Breathable Contact Lens Preservation Products

Domestic

Dates and Status

Aug 06, 2020

Oct 31, 2029