Taiwan FDA registration 6ea3b003cc52e112bf89f09c7481e32f
Kewei nerve stimulation electrode patch
TW: 可威神經刺激電極貼片
Taiwan·Risk Class 2·AXELGAARD MANUFACTURING CO., LTD·Registered May 01, 2007 – May 01, 2012CancelledRegistration details
- Analysis ID
- 6ea3b003cc52e112bf89f09c7481e32f
- Customs Code
- DHA00601804706
Company information
- Manufacturer
- AXELGAARD MANUFACTURING CO., LTD
- Manufacturer Country
- United States
- Authorized Representative
- UNION COMMONWAY INTERNATIONAL CORP.
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.1320 Skin electrode
- Import Information
- import
Dates and status
- Registration Date
- May 01, 2007
- Expiry Date
- May 01, 2012
- Cancellation Date
- Apr 03, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Kewei nerve stimulation electrode patch in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6ea3b003cc52e112bf89f09c7481e32f and manufactured by AXELGAARD MANUFACTURING CO., LTD. The authorized representative in Taiwan is UNION COMMONWAY INTERNATIONAL CORP..
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