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“HOYA” corrective spectacle lens (Non-Sterile) - Taiwan Registration 12ed382ffda8584845e8c5e93665b73a

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 12ed382ffda8584845e8c5e93665b73a 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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12ed382ffda8584845e8c5e93665b73a
Registration Details
Taiwan FDA Registration: 12ed382ffda8584845e8c5e93665b73a
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Device Details

“HOYA” corrective spectacle lens (Non-Sterile)
TW: “豪雅光學”矯正鏡片 (未滅菌)
Risk Class 1
MD

Registration Details

12ed382ffda8584845e8c5e93665b73a

Ministry of Health Medical Device Import No. 022730

DHA09402273006

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

M5844 corrective lenses

Imported from abroad

Dates and Status

Jan 14, 2022

Jan 14, 2027

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