Taiwan FDA registration 7f19cb5e9d8b5ceeac7e856da5208b21

Helium-neon laser

TW: 氦氖雷射
Taiwan flagTaiwan·Risk Class 2·WELLONG INSTRUMENTS CO., LTD.·Registered Sep 28, 2000 – Sep 28, 2025Expired
Registration details
Analysis ID
7f19cb5e9d8b5ceeac7e856da5208b21
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
WELLONG INSTRUMENTS CO., LTD.
Product details
Product Type (Level 1)
9999 Other
Import Information
Domestic
Dates and status
Registration Date
Sep 28, 2000
Expiry Date
Sep 28, 2025
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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 7f19cb5e9d8b5ceeac7e856da5208b21 and manufactured by WELLONG INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is WELLONG INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including TAIEX 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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