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Fujita Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration b314527bf4d876cb24c85215b62345ff

Access comprehensive regulatory information for Fujita Corrective Spectacle Lens (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b314527bf4d876cb24c85215b62345ff and manufactured by FUJITA OPTICAL CO., LTD.. The authorized representative in Taiwan is EMIN OPTICAL 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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b314527bf4d876cb24c85215b62345ff
Registration Details
Taiwan FDA Registration: b314527bf4d876cb24c85215b62345ff
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Device Details

Fujita Corrective Spectacle Lens (Non-Sterile)
TW: ่—ค็”ฐ ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

b314527bf4d876cb24c85215b62345ff

Ministry of Health Medical Device Import No. 016368

DHA09401636803

Company Information

Japan

Product Details

M Ophthalmic devices

M5844 corrective lenses

Imported from abroad

Dates and Status

Apr 08, 2016

Apr 08, 2021

Aug 31, 2023

Cancellation Information

Logged out

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