Taiwan FDA registration 59f9cefd13769b5fdfe75f5e19e03e8b
Helium-neon laser accessory (single-use fiber optic needle)
TW: “敬煇”氦氖雷射附件 (一次性使用光纖針)
Taiwan·Risk Class 2·TAIEX CO., LTD.·Registered Nov 16, 2009 – Nov 16, 2029ActiveRegistration details
- Analysis ID
- 59f9cefd13769b5fdfe75f5e19e03e8b
- Customs Code
- DHY00500283300
Company information
- Manufacturer
- TAIEX CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIEX 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
- Product Type (Level 2)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- Domestic
Dates and status
- Registration Date
- Nov 16, 2009
- Expiry Date
- Nov 16, 2029
About this record
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..
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