Taiwan FDA registration 49be4c4633247d98c96eb5beef3c24f9
"Kadio Sonis" Guantis blood flow meter
TW: "卡迪歐索尼斯"冠提斯血流量測定儀
Taiwan·Risk Class 2·CARDIOSONIX, LTD.·Registered Sep 27, 2006 – Sep 27, 2011CancelledRegistration details
- Analysis ID
- 49be4c4633247d98c96eb5beef3c24f9
- Customs Code
- DHA00601732707
Company information
- Manufacturer
- CARDIOSONIX, LTD.
- Manufacturer Country
- United States
- Authorized Representative
- RAYING TECHNOLOGY COMPANY
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.2100 心血管血流計
- Import Information
- import
Dates and status
- Registration Date
- Sep 27, 2006
- Expiry Date
- Sep 27, 2011
- Cancellation Date
- Nov 16, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kadio Sonis" Guantis blood flow meter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 49be4c4633247d98c96eb5beef3c24f9 and manufactured by CARDIOSONIX, LTD.. The authorized representative in Taiwan is RAYING TECHNOLOGY COMPANY.
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