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“HOYA optical” Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration e987a315cf3a015b5d0720e9b2ec6db0

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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e987a315cf3a015b5d0720e9b2ec6db0
Registration Details
Taiwan FDA Registration: e987a315cf3a015b5d0720e9b2ec6db0
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Device Details

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

Registration Details

e987a315cf3a015b5d0720e9b2ec6db0

Ministry of Health Medical Device Import No. 020955

DHA09402095507

Company Information

Philippines

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

Oct 16, 2019

Oct 16, 2024

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