Taiwan FDA registration 260def2b5500433b32a5cb0341f28cca
“NORAXON” Biofeedback System
TW: “諾克森”生理回饋系統
Taiwan·Risk Class 2·MD·Noraxon USA, Inc.·Registered Nov 28, 2014 – Nov 28, 2024ExpiredRegistration details
- Analysis ID
- 260def2b5500433b32a5cb0341f28cca
- License Form
- Ministry of Health Medical Device Import No. 026800
- Customs Code
- DHA05602680001
Company information
- Manufacturer
- Noraxon USA, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- AMPLE MEDICAL INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K5050 Physiological Feedback Meter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 28, 2014
- Expiry Date
- Nov 28, 2024
About this record
Access comprehensive regulatory information for “NORAXON” Biofeedback System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 260def2b5500433b32a5cb0341f28cca and manufactured by Noraxon USA, Inc.. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS CO., LTD..
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