Taiwan FDA registration aa56d28f681217c038bc319d8b3c0a0d
“Technomed Europe” Disposable Subdermal Needle Electrodes
TW: “泰克諾美特”拋棄式皮下針狀電極
Taiwan·Risk Class 2·MD·TECHNOMED EUROPE·Registered Jul 11, 2019 – Jul 11, 2024ExpiredRegistration details
- Analysis ID
- aa56d28f681217c038bc319d8b3c0a0d
- License Form
- Ministry of Health Medical Device Import No. 032737
- Customs Code
- DHA05603273706
Company information
- Manufacturer
- TECHNOMED EUROPE
- Manufacturer Country
- Netherlands
- Authorized Representative
- SYNGROWTH 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
- Jul 11, 2019
- Expiry Date
- Jul 11, 2024
About this record
Access comprehensive regulatory information for “Technomed Europe” Disposable 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 aa56d28f681217c038bc319d8b3c0a0d and manufactured by TECHNOMED EUROPE. The authorized representative in Taiwan is SYNGROWTH CO., LTD..
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