Taiwan FDA registration fed137af865e594edb20ca9bc2e509f7
Immediate confirmation of the cell membrane glycoprotein receptor IIb/IIIa assay set
TW: 立即確認 細胞膜醣蛋白接受器 IIb/IIIa檢測試劑組
Registration details
- Analysis ID
- fed137af865e594edb20ca9bc2e509f7
- Customs Code
- DHA00602195104
Company information
- Manufacturer
- ACCUMETRICS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- MEDDRAGON TECHNOLOGY CO., LTD.
Product details
- Intended Use
- 立即確認 細胞膜醣蛋白接受器 IIb/IIIa檢測試劑組是一種半定量式全血中血小板功能檢測,測量病人以abciximab或eptifibatide治療後細胞膜醣蛋白接受器 IIb/IIIa的阻斷情形. 臨床醫師於判讀VerifyNow IIb/IIIa assay時應該配合其他臨床與實驗室數據.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.5700 Automated platelet agglutination system
- Import Information
- import
Dates and status
- Registration Date
- Mar 03, 2011
- Expiry Date
- Mar 03, 2016
- Cancellation Date
- May 17, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Immediate confirmation of the cell membrane glycoprotein receptor IIb/IIIa assay set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fed137af865e594edb20ca9bc2e509f7 and manufactured by ACCUMETRICS, INC.. The authorized representative in Taiwan is MEDDRAGON TECHNOLOGY CO., LTD..
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