Taiwan FDA registration f577f5a06706fd4ff00a9418904212cf
"Changan" helium-neon laser accessory
TW: "長安" 氦氖雷射附件
Taiwan·Risk Class 2·WELLONG INSTRUMENTS CO., LTD.·Registered Oct 24, 2005 – Oct 24, 2025ExpiredRegistration details
- Analysis ID
- f577f5a06706fd4ff00a9418904212cf
Company information
- Manufacturer
- WELLONG INSTRUMENTS CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- WELLONG INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 24, 2005
- Expiry Date
- Oct 24, 2025
About this record
Access comprehensive regulatory information for "Changan" helium-neon laser accessory in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f577f5a06706fd4ff00a9418904212cf and manufactured by WELLONG INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is WELLONG INSTRUMENTS CO., LTD..
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