Taiwan FDA registration 9eb45d5bdc642aa80a1c218bb3c82b82
"Diast" IgA Anti-Body Test Set (Unextinguished)
TW: "迪雅仕" 可錄思砂眼披衣菌 IgA 抗體檢測試劑組 (未滅菌)
Taiwan·Risk Class 1·DIESSE DIAGNOSTICA SENESE S.P.A.·Registered Jul 08, 2024 – Jul 08, 2029ActiveRegistration details
- Analysis ID
- 9eb45d5bdc642aa80a1c218bb3c82b82
- Customs Code
- DHA09402353105
Company information
- Manufacturer
- DIESSE DIAGNOSTICA SENESE S.P.A.
- Manufacturer Country
- Italy
- Authorized Representative
- GRAND MARQUIS CO., LTD.
Product details
- Intended Use
- It is limited to the first-level identification scope of Chlamydia serum reagent (C.3120) in the classification and grading management measures for medical devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3120 披衣菌血清試劑
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jul 08, 2024
- Expiry Date
- Jul 08, 2029
About this record
Access comprehensive regulatory information for "Diast" IgA Anti-Body Test Set (Unextinguished) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9eb45d5bdc642aa80a1c218bb3c82b82 and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
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