Taiwan FDA registration 227904b81ce5cfa002e12e8f8af3d020
Emmett Low Frequency Therapy Device
TW: 艾美特低周波治療器
Taiwan·Risk Class 2·TUNG FU ELECTRIC CO., LTD.·Registered Dec 05, 2008 – Dec 05, 2013CancelledRegistration details
- Analysis ID
- 227904b81ce5cfa002e12e8f8af3d020
- Customs Code
- DHY00500256208
Company information
- Manufacturer
- TUNG FU ELECTRIC CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TUNG FU ELECTRIC 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
- Domestic
Dates and status
- Registration Date
- Dec 05, 2008
- Expiry Date
- Dec 05, 2013
- Cancellation Date
- Aug 12, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Emmett 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 227904b81ce5cfa002e12e8f8af3d020 and manufactured by TUNG FU ELECTRIC CO., LTD.. The authorized representative in Taiwan is TUNG FU ELECTRIC CO., LTD..
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