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"Chengxian" multi-wavelength medical laser therapy instrument - Taiwan Registration 05b31f78fcb2fcd65d01ebc2097cfaeb

Access comprehensive regulatory information for "Chengxian" multi-wavelength medical laser therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 05b31f78fcb2fcd65d01ebc2097cfaeb 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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05b31f78fcb2fcd65d01ebc2097cfaeb
Registration Details
Taiwan FDA Registration: 05b31f78fcb2fcd65d01ebc2097cfaeb
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Device Details

"Chengxian" multi-wavelength medical laser therapy instrument
TW: โ€œๆ‰ฟ่ณขโ€ๅคšๆณข้•ท้†ซ็”จ้›ทๅฐ„ๆฒป็™‚ๅ„€
Risk Class 2
Cancelled

Registration Details

05b31f78fcb2fcd65d01ebc2097cfaeb

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

Nov 27, 2012

Nov 27, 2017

Nov 26, 2019

Cancellation Information

Logged out

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