Taiwan FDA registration c8617271ee11abc82b69908b0186bac4
Likang medium frequency pulse therapy instrument
TW: 利康中頻脈衝治療儀
Taiwan·Risk Class 2·T.Y. SHERRY INTERNATIONAL CO., LTD.·Registered Feb 23, 2009 – May 27, 2019CancelledRegistration details
- Analysis ID
- c8617271ee11abc82b69908b0186bac4
- Customs Code
- DHY00500264400
Company information
- Manufacturer
- T.Y. SHERRY INTERNATIONAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- T.Y. SHERRY INTERNATIONAL 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
- Feb 23, 2009
- Expiry Date
- May 27, 2019
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Likang medium frequency pulse therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c8617271ee11abc82b69908b0186bac4 and manufactured by T.Y. SHERRY INTERNATIONAL CO., LTD.. The authorized representative in Taiwan is T.Y. SHERRY INTERNATIONAL CO., LTD..
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