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NEOS Corrective Spectacle Lens (Non-sterile) - Taiwan Registration e82c9e8208629502f06408f75b5994ea

Access comprehensive regulatory information for NEOS 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 e82c9e8208629502f06408f75b5994ea and manufactured by NIKON ESSILOR CO., LTD.. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN 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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e82c9e8208629502f06408f75b5994ea
Registration Details
Taiwan FDA Registration: e82c9e8208629502f06408f75b5994ea
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Device Details

NEOS Corrective Spectacle Lens (Non-sterile)
TW: ๅฐผๆญ ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

e82c9e8208629502f06408f75b5994ea

Ministry of Health Medical Device Import No. 017439

DHA09401743905

Company Information

Japan

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".

M Ophthalmic devices

M5844 corrective lenses

Imported from abroad

Dates and Status

Jan 19, 2017

Jan 19, 2027