Magnesium Quantitative Testing Drug - Vietnam Registration 240000263/PCBB-HN

Access comprehensive regulatory information for Magnesium Quantitative Testing Drug 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 240000263/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 Roche Diagnostics GmbH, Theo phụ lục, 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.

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240000263/PCBB-HN

Registration Details

Vietnam MOH Registration: 240000263/PCBB-HN

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Device Details

Magnesium Quantitative Testing Drug

VN: Thuốc thử xét nghiệm định lượng Magnesium

Risk Class TTBYT Loại B

Registration Details

Analysis ID

240000263/PCBB-HN

Submission ID

000.00.19.H26-231221-0018

Product Type

Theo theo phụ lục

Product Code

Theo phụ lục

Technical Details

Intended Use

Magnesium testing is used to quantify magnesium in human serum, plasma, or urine on the Alinity c Systems. The measurement of magnesium concentration is used in the diagnosis and treatment of hypomagnesemia (abnormally low magnesium concentration in the blood) and hypermagnesemia (abnormally high magnesium concentration in the blood).