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“HOYA” Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration 7efda029bcdd6f97ca9388b7e490342c

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 7efda029bcdd6f97ca9388b7e490342c and manufactured by HOYA LENS VIETNAM LTD – QUANG NGAI BRANCH. 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 LENS VIETNAM LTD - QUANG NGAI BRANCH, 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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7efda029bcdd6f97ca9388b7e490342c
Registration Details
Taiwan FDA Registration: 7efda029bcdd6f97ca9388b7e490342c
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Device Details

“HOYA” Corrective Spectacle Lens (Non-Sterile)
TW: “豪雅” 矯正鏡片 (未滅菌)
Risk Class 1
MD

Registration Details

7efda029bcdd6f97ca9388b7e490342c

Ministry of Health Medical Device Import No. 022175

DHA09402217504

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

Dates and Status

Dec 11, 2020

Dec 11, 2025

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