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MOSE & DEVICE Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration d3b809af2dd42cfcaadd60d9cdeafe8e

Access comprehensive regulatory information for MOSE & DEVICE 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 d3b809af2dd42cfcaadd60d9cdeafe8e 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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d3b809af2dd42cfcaadd60d9cdeafe8e
Registration Details
Taiwan FDA Registration: d3b809af2dd42cfcaadd60d9cdeafe8e
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Device Details

MOSE & DEVICE Corrective Spectacle Lens (Non-Sterile)
TW: ๆ‘ฉๆ–ฏ ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d3b809af2dd42cfcaadd60d9cdeafe8e

Ministry of Health Medical Device Import No. 020841

DHA09402084105

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

Sep 09, 2019

Sep 09, 2024