Taiwan FDA registration d77bc33d99f2b60c1fa1c0a92b6752ab
Genki Lele Low Frequency Healer
TW: 元氣樂樂低周波治療器
Taiwan·Risk Class 2·Fengmao Technology Co., Ltd. third factory·Registered Aug 14, 2006 – Aug 14, 2011CancelledRegistration details
- Analysis ID
- d77bc33d99f2b60c1fa1c0a92b6752ab
- Customs Code
- DHY00500190405
Company information
- Manufacturer
- Fengmao Technology Co., Ltd. third factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SANKEI 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
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Aug 14, 2006
- Expiry Date
- Aug 14, 2011
- Cancellation Date
- Jan 14, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Genki Lele Low Frequency Healer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d77bc33d99f2b60c1fa1c0a92b6752ab and manufactured by Fengmao Technology Co., Ltd. third factory. The authorized representative in Taiwan is SANKEI CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices