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"Seunghyun" ophthalmic dual-wavelength laser treatment instrument - Taiwan Registration ae1e0ddbfac01674df5363b61ead3366

Access comprehensive regulatory information for "Seunghyun" ophthalmic dual-wavelength laser treatment instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ae1e0ddbfac01674df5363b61ead3366 and manufactured by LIGHTMED CORPORATION. The authorized representative in Taiwan is LIGHTMED CORPORATION.

This page provides complete technical specifications, regulatory compliance details. 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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ae1e0ddbfac01674df5363b61ead3366
Registration Details
Taiwan FDA Registration: ae1e0ddbfac01674df5363b61ead3366
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Device Details

"Seunghyun" ophthalmic dual-wavelength laser treatment instrument
TW: โ€œๆ‰ฟ่ณขโ€็œผ็ง‘้›™ๆณข้•ท้›ทๅฐ„ๆฒป็™‚ๅ„€
Risk Class 2

Registration Details

ae1e0ddbfac01674df5363b61ead3366

DHY00500291005

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmology

M.4390 ็œผ็ง‘้›ทๅฐ„่ฃ็ฝฎ

Domestic

Dates and Status

Mar 24, 2010

Mar 24, 2030