Taiwan FDA registration 996aa9120fda16cb07b1808b23b258ee
“Natus” Nicolet EEG wireless 32/64 Amplifier
TW: “納特斯”尼可腦波無線放大器
Taiwan·Risk Class 2·MD·Natus Neurology Incorporated·Registered Oct 09, 2014 – Oct 09, 2019CancelledRegistration details
- Analysis ID
- 996aa9120fda16cb07b1808b23b258ee
- License Form
- Ministry of Health Medical Device Import No. 026640
- Customs Code
- DHA05602664005
Company information
- Manufacturer
- Natus Neurology Incorporated
- Manufacturer Country
- United States
- Authorized Representative
- SYNGROWTH CO., LTD.
Product details
- 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
- Oct 09, 2014
- Expiry Date
- Oct 09, 2019
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “Natus” Nicolet EEG wireless 32/64 Amplifier in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 996aa9120fda16cb07b1808b23b258ee and manufactured by Natus Neurology Incorporated. The authorized representative in Taiwan is SYNGROWTH CO., LTD..
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