Taiwan FDA registration fd732a58b30be9837606fbbb4bff9d3e
“Neurosoft” Ambulatory EEG and PSG system
TW: “紐羅舒芙特”攜帶式腦波暨多種生理訊號描記器
Taiwan·Risk Class 2·MD·NEUROSOFT LLC.·Registered Aug 30, 2019 – Aug 30, 2024ExpiredRegistration details
- Analysis ID
- fd732a58b30be9837606fbbb4bff9d3e
- License Form
- Ministry of Health Medical Device Import No. 032821
- Customs Code
- DHA05603282108
Company information
- Manufacturer
- NEUROSOFT LLC.
- Manufacturer Country
- Russian Federation
- Authorized Representative
- HOI MEDICAL 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)
- K1400 brainwave scanner
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 30, 2019
- Expiry Date
- Aug 30, 2024
About this record
Access comprehensive regulatory information for “Neurosoft” Ambulatory EEG and PSG system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fd732a58b30be9837606fbbb4bff9d3e and manufactured by NEUROSOFT LLC.. The authorized representative in Taiwan is HOI MEDICAL CO., LTD..
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