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Helium-neon laser - Taiwan Registration d0600b604f1b2a3efd15f4436869aa78

Access comprehensive regulatory information for Helium-neon laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d0600b604f1b2a3efd15f4436869aa78 and manufactured by TAIEX CO., LTD.. The authorized representative in Taiwan is TAIEX CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including WELLONG INSTRUMENTS CO., LTD., NEEDLELESS CORPORATION, and 5 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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d0600b604f1b2a3efd15f4436869aa78
Registration Details
Taiwan FDA Registration: d0600b604f1b2a3efd15f4436869aa78
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Device Details

Helium-neon laser
TW: ๆฐฆๆฐ–้›ทๅฐ„
Risk Class 2

Registration Details

d0600b604f1b2a3efd15f4436869aa78

DHY00500077400

Company Information

Taiwan, Province of China

Product Details

2199 Other medical laser devices

Domestic

Dates and Status

Apr 21, 1999

Feb 09, 2029