Taiwan FDA registration d0600b604f1b2a3efd15f4436869aa78

Helium-neon laser

TW: 氦氖雷射
Taiwan flagTaiwan·Risk Class 2·TAIEX CO., LTD.·Registered Apr 21, 1999 – Feb 09, 2029Active
Registration details
Analysis ID
d0600b604f1b2a3efd15f4436869aa78
Customs Code
DHY00500077400
Company information
Manufacturer
TAIEX CO., LTD.
Manufacturer Country
Taiwan, Province of China
Authorized Representative
TAIEX CO., LTD.
Product details
Product Type (Level 1)
2199 Other medical laser devices
Import Information
Domestic
Dates and status
Registration Date
Apr 21, 1999
Expiry Date
Feb 09, 2029
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About this record

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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