Taiwan FDA registration 3c12a2b73ff38f05c9e600cd5b254e19
"Hongtai" ultrasound diathermy therapy device
TW: "虹泰" 超音波透熱治療儀
Taiwan·Risk Class 2·Hongtai Enterprise Co., Ltd. Rende Factory·Registered Jun 23, 2005 – Jun 23, 2025ExpiredRegistration details
- Analysis ID
- 3c12a2b73ff38f05c9e600cd5b254e19
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)
- o Physical Medical Sciences
- Import Information
- Domestic
Dates and status
- Registration Date
- Jun 23, 2005
- Expiry Date
- Jun 23, 2025
About this record
Access comprehensive regulatory information for "Hongtai" ultrasound diathermy 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 3c12a2b73ff38f05c9e600cd5b254e19 and manufactured by Hongtai Enterprise Co., Ltd. Rende Factory. The authorized representative in Taiwan is HOME CARE TECHNOLOGY 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