Taiwan FDA registration 8d9a938d5aab17b30212c5409be9a276
“Everyway” Transcutaneous Electrical Nerve Stimulator
TW: “醫樺”經皮神經電刺激器
Taiwan·Risk Class 2·MD·EVERYWAY MEDICAL INSTRUMENTS CO., LTD.·Registered Feb 24, 2014 – Feb 24, 2024ExpiredRegistration details
- Analysis ID
- 8d9a938d5aab17b30212c5409be9a276
- License Form
- Ministry of Health Medical Device Manufacturing No. 004493
Company information
- Manufacturer
- EVERYWAY MEDICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- EVERYWAY MEDICAL INSTRUMENTS 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)
- K5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Feb 24, 2014
- Expiry Date
- Feb 24, 2024
About this record
Access comprehensive regulatory information for “Everyway” Transcutaneous Electrical Nerve Stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8d9a938d5aab17b30212c5409be9a276 and manufactured by EVERYWAY MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is EVERYWAY MEDICAL INSTRUMENTS CO., LTD..
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