Taiwan FDA registration ff22a04ee9971ff1fb849a6bb7075422
“Neurosign” IOM Stimulation Probe
TW: “紐倫帥”刺激探頭
Taiwan·Risk Class 2·MD·TECHNOMED EUROPE·Registered Oct 18, 2022 – Oct 18, 2027ActiveRegistration details
- Analysis ID
- ff22a04ee9971ff1fb849a6bb7075422
- License Form
- Ministry of Health Medical Device Import No. 035939
- Customs Code
- DHA05603593907
Company information
- Manufacturer
- TECHNOMED EUROPE
- Manufacturer Country
- Netherlands
- Authorized Representative
- TRUSHINE MEDICAL INSTRUMENT CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G1820 Surgical neurostimulator/positioner
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 18, 2022
- Expiry Date
- Oct 18, 2027
About this record
Access comprehensive regulatory information for “Neurosign” IOM Stimulation Probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ff22a04ee9971ff1fb849a6bb7075422 and manufactured by TECHNOMED EUROPE. The authorized representative in Taiwan is TRUSHINE MEDICAL INSTRUMENT CO., LTD..
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