Taiwan FDA registration e987a315cf3a015b5d0720e9b2ec6db0

“HOYA optical” Corrective Spectacle Lens (Non-Sterile)

TW: “台灣頂點” 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·EHS LENS PHILIPPINES, INC.·Registered Oct 16, 2019 – Oct 16, 2024Expired
Registration details
Analysis ID
e987a315cf3a015b5d0720e9b2ec6db0
License Form
Ministry of Health Medical Device Import No. 020955
Customs Code
DHA09402095507
Company information
Manufacturer Country
Philippines
Authorized Representative
MEGANEICHIBA TAIWAN CO., 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
Oct 16, 2019
Expiry Date
Oct 16, 2024
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About this record

Access comprehensive regulatory information for “HOYA optical” 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 e987a315cf3a015b5d0720e9b2ec6db0 and manufactured by EHS LENS PHILIPPINES, INC.. The authorized representative in Taiwan is MEGANEICHIBA TAIWAN CO., 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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