Taiwan FDA registration d67828fca12f34b696d0b8039cdacf98
"Medtronic" recalcified activates the solidified timing cassette
TW: "美敦力"再鈣化活化凝固計時卡匣
Taiwan·Risk Class 2·MEDTRONIC PERFUSION SYSTEMS·Registered Mar 14, 2006 – Mar 14, 2016CancelledRegistration details
- Analysis ID
- d67828fca12f34b696d0b8039cdacf98
- Customs Code
- DHA00601614002
Company information
- Manufacturer
- MEDTRONIC PERFUSION SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- Used to determine activation coagulation time of whole blood.
- 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" recalcified activates the solidified timing cassette in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d67828fca12f34b696d0b8039cdacf98 and manufactured by MEDTRONIC PERFUSION SYSTEMS. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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