Taiwan FDA registration fe7105926354c9c2dfd87a043a51a9fb
Funai Biomedical Low Frequency Therapy Device
TW: 船井生醫低週波治療器
Taiwan·Risk Class 2·Hongtai Enterprise Co., Ltd. Rende Factory·Registered Apr 27, 2010 – Aug 12, 2016CancelledRegistration details
- Analysis ID
- fe7105926354c9c2dfd87a043a51a9fb
- Customs Code
- DHY00500292505
Company information
- Manufacturer
- Hongtai Enterprise Co., Ltd. Rende Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Hongtai Enterprise Co., Ltd. Rende Factory
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
- Domestic
Dates and status
- Registration Date
- Apr 27, 2010
- Expiry Date
- Aug 12, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Funai Biomedical 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 fe7105926354c9c2dfd87a043a51a9fb and manufactured by Hongtai Enterprise Co., Ltd. Rende Factory. The authorized representative in Taiwan is Hongtai Enterprise Co., Ltd. Rende Factory.
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