Taiwan FDA registration 7efda029bcdd6f97ca9388b7e490342c

“HOYA” Corrective Spectacle Lens (Non-Sterile)

TW: “豪雅” 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·HOYA LENS VIETNAM LTD – QUANG NGAI BRANCH·Registered Dec 11, 2020 – Dec 11, 2025Expired
Registration details
Analysis ID
7efda029bcdd6f97ca9388b7e490342c
License Form
Ministry of Health Medical Device Import No. 022175
Customs Code
DHA09402217504
Company information
Manufacturer Country
Viet Nam
Authorized Representative
HOYA LENS TAIWAN LTD.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M5844 corrective lenses
Import Information
Imported from abroad
Dates and status
Registration Date
Dec 11, 2020
Expiry Date
Dec 11, 2025
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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 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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