Taiwan FDA registration afa72a43cf6efeb8865b4a02c820e23e
禮雅尚 EB 病毒早期抗原 IgG 檢測試劑-品管液
Taiwan·Risk Class 2·DIASORIN ITALIA S.P.A.·Registered Dec 25, 2023 – Dec 25, 2028ActiveRegistration details
- Analysis ID
- afa72a43cf6efeb8865b4a02c820e23e
- Customs Code
- DHA05603624505
Company information
- Manufacturer
- DIASORIN ITALIA S.P.A.
- Manufacturer Country
- Italy
- Authorized Representative
- MEDRICH INSTRUMENT CO., LTD.
Product details
- Intended Use
- This product (negative and positive) is used to confirm the efficacy of the Epstein-Barr Virus Early Antigen IgG Detection Reagent on the Liashan Chemical Cold Light Immunoassay Analyzer.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Dec 25, 2023
- Expiry Date
- Dec 25, 2028
About this record
Access comprehensive regulatory information for 禮雅尚 EB 病毒早期抗原 IgG 檢測試劑-品管液 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number afa72a43cf6efeb8865b4a02c820e23e and manufactured by DIASORIN ITALIA S.P.A.. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..
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