Taiwan FDA registration 856f8b36814855f60cc9831278dc5df3
Lycra low-frequency therapy device
TW: 萊卡低週波治療器
Taiwan·Risk Class 2·Hongtai Enterprise Co., Ltd. Rende Factory·Registered Sep 14, 2005 – Aug 12, 2006CancelledRegistration details
- Analysis ID
- 856f8b36814855f60cc9831278dc5df3
- Customs Code
- DHY00500144805
Company information
- Manufacturer
- Hongtai Enterprise Co., Ltd. Rende Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HOME CARE TECHNOLOGY 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
- Sep 14, 2005
- Expiry Date
- Aug 12, 2006
- Cancellation Date
- Nov 27, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Lycra 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 856f8b36814855f60cc9831278dc5df3 and manufactured by Hongtai Enterprise Co., Ltd. Rende Factory. The authorized representative in Taiwan is HOME CARE TECHNOLOGY CO., LTD..
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