Taiwan FDA registration 24af55d3c514369e41f077aa41ca45cb
"歐姆龍" knee low frequency therapy device
TW: “歐姆龍”膝用低周波治療器
Taiwan·Risk Class 2·OMRON DALIAN CO., LTD.;; OMRON HEALTHCARE CO., LTD.·Registered Mar 13, 2021 – Mar 13, 2026ExpiredRegistration details
- Analysis ID
- 24af55d3c514369e41f077aa41ca45cb
- Customs Code
- DHA09200121407
Company information
- Manufacturer Country
- Japan;;China
- 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 Neuroscience
- Product Type (Level 2)
- K.5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- Input;; Contract manufacturing;; Chinese goods
Dates and status
- Registration Date
- Mar 13, 2021
- Expiry Date
- Mar 13, 2026
About this record
Access comprehensive regulatory information for "歐姆龍" knee low frequency therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 24af55d3c514369e41f077aa41ca45cb and manufactured by OMRON DALIAN CO., LTD.;; OMRON HEALTHCARE CO., LTD.. The authorized representative in Taiwan is OMRON HEALTHCARE TAIWAN CO., LTD..
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