Taiwan FDA registration 30a6b9ff6bac7cfd599b46a86816bbed
Abbott "Marisi" Human immunodeficiency virus antigen and antibody test reagent
TW: 亞培"妙芮絲" 人類免疫缺乏病毒抗原及抗體檢驗試劑
Taiwan·Risk Class 3·DIASORIN S.P.A. UK BRANCH·Registered Jul 02, 2004 – Jul 02, 2024ExpiredRegistration details
- Analysis ID
- 30a6b9ff6bac7cfd599b46a86816bbed
- Customs Code
- DHA00601074006
Company information
- Manufacturer
- DIASORIN S.P.A. UK BRANCH
- Manufacturer Country
- United Kingdom
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- Enzyme immunoassay for enhancing human immunodeficiency virus type 1 (HIV-1. HIV-1 O) and type 2 (HIV-2) detection.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Import Information
- import
Dates and status
- Registration Date
- Jul 02, 2004
- Expiry Date
- Jul 02, 2024
About this record
Access comprehensive regulatory information for Abbott "Marisi" Human immunodeficiency virus antigen and antibody test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 30a6b9ff6bac7cfd599b46a86816bbed and manufactured by DIASORIN S.P.A. UK BRANCH. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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