Taiwan FDA registration e3791fcb28be2424806c2bcb02bbe819
"Red Yang" low-frequency therapy device
TW: "紅陽" 低週波治療器
Registration details
- Analysis ID
- e3791fcb28be2424806c2bcb02bbe819
- Customs Code
- DHY00500092001
Company information
- Manufacturer
- SUN-RAIN SYSTEM CORP.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SUN-RAIN SYSTEM CORP.
Product details
- Product Type (Level 1)
- K000 Neuroscience
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 04, 2001
- Expiry Date
- Jul 10, 2017
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Red Yang" 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 e3791fcb28be2424806c2bcb02bbe819 and manufactured by SUN-RAIN SYSTEM CORP.. The authorized representative in Taiwan is SUN-RAIN SYSTEM CORP..
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.
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