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"Flyshuttle" corrective lenses (unsterilized) - Taiwan Registration dee900b40bc76b50edc3975c20964e74

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 dee900b40bc76b50edc3975c20964e74 and manufactured by CHEMIGLAS CORPORATION. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including ESSILOR MANUFACTURING (THAILAND) CO., LTD., 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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dee900b40bc76b50edc3975c20964e74
Registration Details
Taiwan FDA Registration: dee900b40bc76b50edc3975c20964e74
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Device Details

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

Registration Details

dee900b40bc76b50edc3975c20964e74

DHA04400906208

Company Information

Korea, Republic of

Product Details

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

M Ophthalmology

M.5844 corrective lenses

import

Dates and Status

Aug 10, 2010

Aug 10, 2020

Jun 16, 2022

Cancellation Information

Logged out

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