Taiwan FDA registration 45cdb8b23705003f9aded08f492c2658
"Medtronic" high-range heparin/test cassette
TW: "美敦力" 高範圍肝素/試驗卡匣
Taiwan·Risk Class 2·MEDTRONIC PERFUSION SYSTEMS·Registered Mar 14, 2006 – Mar 14, 2016CancelledRegistration details
- Analysis ID
- 45cdb8b23705003f9aded08f492c2658
- Customs Code
- DHA00601614101
Company information
- Manufacturer
- MEDTRONIC PERFUSION SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- The presence of heparin is identified by activating the coagulation time.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.5425 Versatile system for in vitro agglutination studies
- Import Information
- import
Dates and status
- Registration Date
- Mar 14, 2006
- Expiry Date
- Mar 14, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Medtronic" high-range heparin/test cassette in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 45cdb8b23705003f9aded08f492c2658 and manufactured by MEDTRONIC PERFUSION SYSTEMS. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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