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DIAMOND Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration aaeff898dc19cb90c9e7d7eaebb94a1a

Access comprehensive regulatory information for DIAMOND 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 aaeff898dc19cb90c9e7d7eaebb94a1a and manufactured by HONG KONG OPTICAL LENS CO., LTD.. The authorized representative in Taiwan is HKO OPTICAL LENS (TAIWAN) CO., LTD..

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aaeff898dc19cb90c9e7d7eaebb94a1a
Registration Details
Taiwan FDA Registration: aaeff898dc19cb90c9e7d7eaebb94a1a
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Device Details

DIAMOND Corrective Spectacle Lens (Non-Sterile)
TW: ๆ™ถ้‘ฝ ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

aaeff898dc19cb90c9e7d7eaebb94a1a

Ministry of Health Medical Device Import No. 020505

DHA09402050502

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

May 30, 2019

May 30, 2024