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NGK Corrective Spectacle Lens(Non-Sterile) - Taiwan Registration d4bb58d027dc76f18d5e71e2a279e691

Access comprehensive regulatory information for NGK 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 d4bb58d027dc76f18d5e71e2a279e691 and manufactured by NIPPON OPHTHALMIC CO., LTD.. The authorized representative in Taiwan is HKO OPTICAL LENS (TAIWAN) CO., LTD..

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d4bb58d027dc76f18d5e71e2a279e691
Registration Details
Taiwan FDA Registration: d4bb58d027dc76f18d5e71e2a279e691
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Device Details

NGK Corrective Spectacle Lens(Non-Sterile)
TW: ๆ—ฅๆœฌ็œผ้กๅ…‰ๅญธ ็Ÿฏๆญฃ้ก็‰‡(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d4bb58d027dc76f18d5e71e2a279e691

Ministry of Health Medical Device Import No. 022454

DHA09402245408

Company Information

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

Apr 08, 2021

Apr 08, 2026