Taiwan FDA registration 20aed63989796da9d8ea8916f73f229e
Inmeis eight-channel brain wave machine
TW: 映美思八通道腦波機
Taiwan·Risk Class 2·Weifeng Technology Co., Ltd·Registered Oct 25, 2024 – Oct 25, 2029ActiveRegistration details
- Analysis ID
- 20aed63989796da9d8ea8916f73f229e
Company information
- Manufacturer
- Weifeng Technology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Weifeng Technology Co., Ltd
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.1400 Brain Wave Scanner
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 25, 2024
- Expiry Date
- Oct 25, 2029
About this record
Access comprehensive regulatory information for Inmeis eight-channel brain wave machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 20aed63989796da9d8ea8916f73f229e and manufactured by Weifeng Technology Co., Ltd. The authorized representative in Taiwan is Weifeng Technology Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. 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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