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Optovision Corrective Spectacle Lens(Non-Sterile) - Taiwan Registration 4979136952bfc1aa84df1ea6d3cb4706

Access comprehensive regulatory information for Optovision 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 4979136952bfc1aa84df1ea6d3cb4706 and manufactured by HONG KONG OPTICAL LENS CO., LTD.. The authorized representative in Taiwan is HKO OPTICAL LENS (TAIWAN) CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including OptoVision GERMANY, 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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4979136952bfc1aa84df1ea6d3cb4706
Registration Details
Taiwan FDA Registration: 4979136952bfc1aa84df1ea6d3cb4706
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Device Details

Optovision Corrective Spectacle Lens(Non-Sterile)
TW: ๆญ็‰น ็Ÿฏๆญฃ้ก็‰‡
Risk Class 1
MD

Registration Details

4979136952bfc1aa84df1ea6d3cb4706

Ministry of Health Medical Device Import No. 022830

DHA09402283000

Company Information

Product Details

Limited to the first level identification scope of the "corrective lenses (M.5844)" of the Measures for the Classification and Grading of Medical Equipment.

M Ophthalmology

M5844 corrective lenses

Imported from abroad

Dates and Status

Jun 17, 2022

Jun 17, 2027

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