Quantitative uric acid test reagent
Vietnam·Risk Class TTBYT Loại B·Theo theo phụ lục·Registered Apr 24, 2024- Analysis ID
- 240000906/PCBB-HN
- Submission ID
- 000.00.19.H26-240313-0002
- Product Type
- Theo theo phụ lục
- Product Code
- Theo phụ lục
- Authorized Representative
- VĂN PHÒNG ĐẠI DIỆN ABBOTT LABORATORIES GMBH TẠI THÀNH PHỐ HÀ NỘI
- Intended Use
- The Uric Acid2 test is used to quantify uric acid in human serum, plasma, or urine on the Alinity c system. The Uric Acid2 test is used to support the diagnosis and treatment of various kidney conditions and metabolic disorders, including chronic kidney disease, gout, leukemia, psoriasis, anemia or malnutrition, and patients taking cytotoxic drugs.
- Registration Date
- Apr 24, 2024
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Access comprehensive regulatory information for Quantitative uric acid test reagent in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại B medical device is registered under number 240000906/PCBB-HN. The authorized representative in Vietnam is VĂN PHÒNG ĐẠI DIỆN ABBOTT LABORATORIES GMBH TẠI THÀNH PHỐ HÀ NỘI.
This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Biolabo S.A.S., DIALAB Production and Distribution of Chemical-Technical Products and Laboratory Instruments Gesellschaft m.b.H. (tên viết tắt: DIALAB hoặc DIALAB GmbH), Austria , and 5 recent registrations in the same category. Pure Global AI offers free access to 300,000+ Vietnamese medical device registrations, helping global MedTech companies navigate Vietnam MOH regulations, identify competitors, and discover partnership opportunities efficiently.