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"HOYA" Corrective spectacle lens (Non-Sterile) - Taiwan Registration a0210fda1276676b7fd24799b53c836c

Access comprehensive regulatory information for "HOYA" 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 a0210fda1276676b7fd24799b53c836c and manufactured by DAEJEON DAEMYUNG OPTICAL (HANGZHOU) CO.,LTD.. The authorized representative in Taiwan is HOYA LENS TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HOYA CORPORATION, and 1 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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a0210fda1276676b7fd24799b53c836c
Registration Details
Taiwan FDA Registration: a0210fda1276676b7fd24799b53c836c
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Device Details

"HOYA" Corrective spectacle lens (Non-Sterile)
TW: "่ฑช้›…" ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

a0210fda1276676b7fd24799b53c836c

Ministry of Health Medical Device Land Transport No. 004116

DHA09600411602

Company Information

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; Made in China

Dates and Status

Mar 19, 2020

Mar 19, 2025

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