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Shin Sin Multi-Action Solution - Taiwan Registration c0d9a9ea44a4c5a7204207a1e3f2d013

Access comprehensive regulatory information for Shin Sin Multi-Action Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c0d9a9ea44a4c5a7204207a1e3f2d013 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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c0d9a9ea44a4c5a7204207a1e3f2d013
Registration Details
Taiwan FDA Registration: c0d9a9ea44a4c5a7204207a1e3f2d013
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Device Details

Shin Sin Multi-Action Solution
TW: ่ฆ–ๆ–ฐ็กฌๅผ้ก็‰‡ๅ…จๆ•ˆ่ญท็†ๆถฒ
Risk Class 2
MD

Registration Details

c0d9a9ea44a4c5a7204207a1e3f2d013

Ministry of Health Medical Device Manufacturing No. 005500

Company Information

Taiwan, Province of China

Product Details

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

M Ophthalmic devices

M5918 Rigid breathable contact lens preservation product

Produced in Taiwan, China

Dates and Status

Oct 04, 2016

Oct 12, 2025