Taiwan FDA registration 448b7f2ce5b1df1f038169b6474f2f04
"Magic Control" protamine dosimetry
TW: “奇魔控”魚精蛋白劑量測定
Taiwan·Risk Class 2·Accriva Diagnostics Inc., dba ITC, dba Accumetrics·Registered May 23, 2007 – May 23, 2022CancelledRegistration details
- Analysis ID
- 448b7f2ce5b1df1f038169b6474f2f04
- Customs Code
- DHA00601826809
Company information
- Manufacturer Country
- United States
- Authorized Representative
- TRANSMEDIC CO., LTD.
Product details
- Intended Use
- Used to assess protamine dose response in vitro.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.7525 Heparin analysis
- Import Information
- import
Dates and status
- Registration Date
- May 23, 2007
- Expiry Date
- May 23, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Magic Control" protamine dosimetry in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 448b7f2ce5b1df1f038169b6474f2f04 and manufactured by Accriva Diagnostics Inc., dba ITC, dba Accumetrics. The authorized representative in Taiwan is TRANSMEDIC CO., LTD..
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