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"Insight" Light Pulse Dry Eye Treatment Device and its accessories - Taiwan Registration 39fb041c3c21cdb0ebb09ce10c18b040

Access comprehensive regulatory information for "Insight" Light Pulse Dry Eye Treatment Device and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 39fb041c3c21cdb0ebb09ce10c18b040 and manufactured by E-SWIN. The authorized representative in Taiwan is CLINICO INC..

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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39fb041c3c21cdb0ebb09ce10c18b040
Registration Details
Taiwan FDA Registration: 39fb041c3c21cdb0ebb09ce10c18b040
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Device Details

"Insight" Light Pulse Dry Eye Treatment Device and its accessories
TW: โ€œ็›Š่ฆ–โ€ ๅ…‰่„ˆ่กไนพ็œผๆฒป็™‚ๅ„€ๅŠๅ…ถ้…ไปถ
Risk Class 2

Registration Details

39fb041c3c21cdb0ebb09ce10c18b040

DHA05603161908

Company Information

France

Product Details

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

M Ophthalmology

M.9999 Miscellaneous

import

Dates and Status

Dec 12, 2019

Dec 12, 2029