Taiwan FDA registration 36120a3968b5db085d1e1c847cb0a371
“Technomed Europe”Subdermal Needle Electrodes
TW: “鈦克諾美德”皮下針狀電極
Taiwan·Risk Class 2·MD·TECHNOMED EUROPE·Registered Feb 20, 2017 – Feb 20, 2027ActiveRegistration details
- Analysis ID
- 36120a3968b5db085d1e1c847cb0a371
- License Form
- Ministry of Health Medical Device Import No. 029454
- Customs Code
- DHA05602945400
Company information
- Manufacturer
- TECHNOMED EUROPE
- Manufacturer Country
- Netherlands
- Authorized Representative
- TRUSHINE MEDICAL INSTRUMENT 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)
- K1350 Needle Type Electrode
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 20, 2017
- Expiry Date
- Feb 20, 2027
About this record
Access comprehensive regulatory information for “Technomed Europe”Subdermal Needle Electrodes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 36120a3968b5db085d1e1c847cb0a371 and manufactured by TECHNOMED EUROPE. The authorized representative in Taiwan is TRUSHINE MEDICAL INSTRUMENT CO., LTD..
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