Taiwan FDA registration 745ffbcbcf3ccb388d6301015ade1f9c
"Magic Control" activated coagulation time test
TW: "奇魔控" 活化凝血時間試驗
Taiwan·Risk Class 2·Accriva Diagnostics Inc., dba ITC, dba Accumetrics·Registered May 01, 2006 – May 01, 2021CancelledRegistration details
- Analysis ID
- 745ffbcbcf3ccb388d6301015ade1f9c
- Customs Code
- DHA00601649500
Company information
- Manufacturer Country
- United States
- Authorized Representative
- TRANSMEDIC CO., LTD.
Product details
- Intended Use
- Quantitative measurement of heparin in whole blood.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.7140 Activated whole blood coagulation time test
- Import Information
- import
Dates and status
- Registration Date
- May 01, 2006
- Expiry Date
- May 01, 2021
- Cancellation Date
- Dec 08, 2021
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Magic Control" activated coagulation time test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 745ffbcbcf3ccb388d6301015ade1f9c and manufactured by Accriva Diagnostics Inc., dba ITC, dba Accumetrics. The authorized representative in Taiwan is TRANSMEDIC CO., 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