Taiwan FDA registration f68de6befe0f704fe0cac7c26557a914
“OMRON” Electronic Nerve Stimulator electroTHERAPY
TW: “歐姆龍”低周波治療器
Taiwan·Risk Class 2·MD·OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY·Registered Jan 12, 2017 – Jan 12, 2027ActiveRegistration details
- Analysis ID
- f68de6befe0f704fe0cac7c26557a914
- License Form
- Ministry of Health Medical Device Import No. 029341
- Customs Code
- DHA05602934100
Company information
- Manufacturer
- OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- OMRON HEALTHCARE TAIWAN 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
- Imported from abroad
Dates and status
- Registration Date
- Jan 12, 2017
- Expiry Date
- Jan 12, 2027
About this record
Access comprehensive regulatory information for “OMRON” Electronic Nerve Stimulator electroTHERAPY in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f68de6befe0f704fe0cac7c26557a914 and manufactured by OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY. The authorized representative in Taiwan is OMRON HEALTHCARE TAIWAN CO., LTD..
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