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"Flyshuttle" corrective lenses (unsterilized) - Taiwan Registration e2610e506f179f16324d40aadd37fa7a

Access comprehensive regulatory information for "Flyshuttle" corrective lenses (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e2610e506f179f16324d40aadd37fa7a and manufactured by ESSILOR MANUFACTURING (THAILAND) CO., LTD.. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including CHEMIGLAS CORPORATION, ESSILOR-POLYLITE TAIWAN CO., LTD., and 5 recent registrations in the same category. 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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e2610e506f179f16324d40aadd37fa7a
Registration Details
Taiwan FDA Registration: e2610e506f179f16324d40aadd37fa7a
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Device Details

"Flyshuttle" corrective lenses (unsterilized)
TW: โ€œ้ฃ›ๆขญโ€็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

e2610e506f179f16324d40aadd37fa7a

DHA04401099102

Company Information

Product Details

Limited to the first level identification scope of the "corrective lenses (M.5844)" of the Measures for the Classification and Grading of Medical Equipment.

M Ophthalmology

M.5844 corrective lenses

import

Dates and Status

Oct 28, 2011

Oct 28, 2026