Taiwan FDA registration f4820c7b070b423d9c94f0e6944fd7be
"Ruisheng" heart rate variability analyzer
TW: “瑞盛”心率變異分析器
Taiwan·Risk Class 2·Ruisheng Medical Technology Co., Ltd. Zhubei Factory·Registered Apr 14, 2007 – Apr 14, 2012CancelledRegistration details
- Analysis ID
- f4820c7b070b423d9c94f0e6944fd7be
- Customs Code
- DHY00500218708
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ROSSMAX INNOTEK CORP.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.2340 Telecardiogram
- Import Information
- Domestic
Dates and status
- Registration Date
- Apr 14, 2007
- Expiry Date
- Apr 14, 2012
- Cancellation Date
- Apr 14, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ruisheng" heart rate variability analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f4820c7b070b423d9c94f0e6944fd7be and manufactured by Ruisheng Medical Technology Co., Ltd. Zhubei Factory. The authorized representative in Taiwan is ROSSMAX INNOTEK 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.
Free DatabasePowered by Pure Global AI89,000+ Devices