Taiwan FDA registration 7dbcca132dcb64107aa78242de9e90d5
"Diaz" Chlamydomis trachomatis IgG Anti-Body Test Set (Unextinguished)
TW: "迪雅仕" 砂眼披衣菌 IgG 抗體檢測試劑組 (未滅菌)
Taiwan·Risk Class 1·DIESSE DIAGNOSTICA SENESE S.P.A·Registered Aug 08, 2024 – Aug 08, 2029ActiveRegistration details
- Analysis ID
- 7dbcca132dcb64107aa78242de9e90d5
- Customs Code
- DHA09402356101
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
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Aug 08, 2024
- Expiry Date
- Aug 08, 2029
About this record
Access comprehensive regulatory information for "Diaz" Chlamydomis trachomatis IgG 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 7dbcca132dcb64107aa78242de9e90d5 and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
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