Taiwan FDA registration 6602f51d3ba099191198b9004a4f4b3c
Medical card low frequency therapy device
TW: 醫卡低週波治療器
Taiwan·Risk Class 2·Hongtai Enterprise Co., Ltd. Rende Factory·Registered May 16, 2011 – May 16, 2026ExpiredRegistration details
- Analysis ID
- 6602f51d3ba099191198b9004a4f4b3c
- Customs Code
- DHY00500331509
Company information
- Manufacturer
- Hongtai Enterprise Co., Ltd. Rende Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Hongtai Enterprise Co., Ltd. Rende Factory
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
- May 16, 2011
- Expiry Date
- May 16, 2026
About this record
Access comprehensive regulatory information for Medical card 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 6602f51d3ba099191198b9004a4f4b3c and manufactured by Hongtai Enterprise Co., Ltd. Rende Factory. The authorized representative in Taiwan is Hongtai Enterprise Co., Ltd. Rende Factory.
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