Taiwan FDA registration 12ed382ffda8584845e8c5e93665b73a

“HOYA” corrective spectacle lens (Non-Sterile)

TW: “豪雅光學”矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·HOYA LENS VIETNAM LTD - QUANG NGAI BRANCH·Registered Jan 14, 2022 – Jan 14, 2027Active
Registration details
Analysis ID
12ed382ffda8584845e8c5e93665b73a
License Form
Ministry of Health Medical Device Import No. 022730
Customs Code
DHA09402273006
Company information
Manufacturer Country
Viet Nam
Authorized Representative
HOYA LENS TAIWAN LTD.
Product details
Intended Use
Limited to the first level identification scope of the "corrective lenses (M.5844)" of the Measures for the Classification and Grading of Medical Equipment.
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M5844 corrective lenses
Import Information
Imported from abroad
Dates and status
Registration Date
Jan 14, 2022
Expiry Date
Jan 14, 2027
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About this record

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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