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Helium-neon laser accessory (single-use fiber optic needle) - Taiwan Registration 59f9cefd13769b5fdfe75f5e19e03e8b

Access comprehensive regulatory information for Helium-neon laser accessory (single-use fiber optic needle) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 59f9cefd13769b5fdfe75f5e19e03e8b and manufactured by TAIEX CO., LTD.. The authorized representative in Taiwan is TAIEX CO., LTD..

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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59f9cefd13769b5fdfe75f5e19e03e8b
Registration Details
Taiwan FDA Registration: 59f9cefd13769b5fdfe75f5e19e03e8b
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Device Details

Helium-neon laser accessory (single-use fiber optic needle)
TW: โ€œๆ•ฌ็…‡โ€ๆฐฆๆฐ–้›ทๅฐ„้™„ไปถ (ไธ€ๆฌกๆ€งไฝฟ็”จๅ…‰็บ–้‡)
Risk Class 2

Registration Details

59f9cefd13769b5fdfe75f5e19e03e8b

DHY00500283300

Company Information

Taiwan, Province of China

Product Details

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

I General, Plastic Surgery and Dermatology

I.4810 Lasers for general surgical, orthopaedic and dermatological use

Domestic

Dates and Status

Nov 16, 2009

Nov 16, 2029