Taiwan FDA registration 6dbe8fecb9ae36907effd90338ac7d47
“Syneika” Neuronavigator for Transcranial Magnetic Stimulation
TW: “西尼卡”經顱磁刺激導航系統
Taiwan·Risk Class 2·MD·Syneika·Registered Sep 08, 2023 – Sep 08, 2028ActiveRegistration details
- Analysis ID
- 6dbe8fecb9ae36907effd90338ac7d47
- License Form
- Ministry of Health Medical Device Import No. 036725
- Customs Code
- DHA05603672506
Company information
- Manufacturer
- Syneika
- Manufacturer Country
- France
- Authorized Representative
- TRUSHINE MEDICAL INSTRUMENT CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K4560 Instrument for stereotaxic use in the nervous system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 08, 2023
- Expiry Date
- Sep 08, 2028
About this record
Access comprehensive regulatory information for “Syneika” Neuronavigator for Transcranial Magnetic Stimulation in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6dbe8fecb9ae36907effd90338ac7d47 and manufactured by Syneika. The authorized representative in Taiwan is TRUSHINE MEDICAL INSTRUMENT CO., LTD..
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