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Miacare clarion multi-purpose solution - Taiwan Registration 17a00b57f055f613090090c189cf3471

Access comprehensive regulatory information for Miacare clarion multi-purpose solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 17a00b57f055f613090090c189cf3471 and manufactured by NANG KUANG PHARMACEUTICAL CO., LTD.. The authorized representative in Taiwan is BENQ MATERIALS CORP..

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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17a00b57f055f613090090c189cf3471
Registration Details
Taiwan FDA Registration: 17a00b57f055f613090090c189cf3471
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Device Details

Miacare clarion multi-purpose solution
TW: ็พŽ่‹ฅๅบท็›้€ๅคšๆ•ˆไฟ้คŠๆถฒ
Risk Class 2
MD

Registration Details

17a00b57f055f613090090c189cf3471

Ministry of Health Medical Device Manufacturing No. 005539

Company Information

Taiwan, Province of China

Product Details

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

M Ophthalmic devices

M5928 Flexible Contact Lens Preservation

Produced in Taiwan, China

Dates and Status

Nov 10, 2016

Oct 12, 2025