Taiwan FDA registration e174a9b3cf2f26734de09a68689d2352
Quickeli Ji Shortness of breath comprehensive detection reagent
TW: 快得利 揣耶濟 呼吸短促綜合檢測試劑
Taiwan·Risk Class 2·Quidel Cardiovascular Inc.·Registered Feb 23, 2006 – Feb 23, 2026ExpiredRegistration details
- Analysis ID
- e174a9b3cf2f26734de09a68689d2352
- Customs Code
- DHA00601605100
Company information
- Manufacturer
- Quidel Cardiovascular Inc.
- Manufacturer Country
- United States
- Authorized Representative
- BIO-CHECK LABORATORIES LTD.
Product details
- Intended Use
- This product uses EDTA whole blood and plasma samples to quantify CK-MB, myoglobin, Troponin I, BNP and D-DIMER in the Triage machine using fluorescence immunoassay.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1215 Creatine phosphokinase/creatine kinase or isoenzyme testing system
- Import Information
- import
Dates and status
- Registration Date
- Feb 23, 2006
- Expiry Date
- Feb 23, 2026
About this record
Access comprehensive regulatory information for Quickeli Ji Shortness of breath comprehensive detection reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e174a9b3cf2f26734de09a68689d2352 and manufactured by Quidel Cardiovascular Inc.. The authorized representative in Taiwan is BIO-CHECK LABORATORIES LTD..
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