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“HOYA optical” Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration 5b0dc834ec25cb875b69b78212a5f5c9

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 5b0dc834ec25cb875b69b78212a5f5c9 and manufactured by HOYA CORPORATION. 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 EHS LENS PHILIPPINES, INC., 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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5b0dc834ec25cb875b69b78212a5f5c9
Registration Details
Taiwan FDA Registration: 5b0dc834ec25cb875b69b78212a5f5c9
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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

5b0dc834ec25cb875b69b78212a5f5c9

Ministry of Health Medical Device Import No. 020956

DHA09402095609

Company Information

Japan

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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