Taiwan FDA registration 16ee6ecb56f7aa27cd510847547b8ac7
"Medtronic" blood flow rate detection converter
TW: "美敦力" 血液流速偵測轉換器
Taiwan·Risk Class 2·MEDTRONIC PERFUSION SYSTEMS·Registered Sep 14, 2005 – Sep 14, 2025ExpiredRegistration details
- Analysis ID
- 16ee6ecb56f7aa27cd510847547b8ac7
- Customs Code
- DHA00601191201
Company information
- Manufacturer
- MEDTRONIC PERFUSION SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
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.2120 血管外血流探頭
- Import Information
- import
Dates and status
- Registration Date
- Sep 14, 2005
- Expiry Date
- Sep 14, 2025
About this record
Access comprehensive regulatory information for "Medtronic" blood flow rate detection converter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 16ee6ecb56f7aa27cd510847547b8ac7 and manufactured by MEDTRONIC PERFUSION SYSTEMS. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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