Magnesium Quantitative Testing Drug - Vietnam Registration 240002872/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 TBYT Loại B medical device is registered under number 240002872/PCBB-HN and manufactured by Beckman Coulter Ireland Inc.. The authorized representative in Vietnam is CÔNG TY TNHH KỸ THUẬT NAM PHƯƠNG.

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including Theo phụ lục, Roche Diagnostics GmbH, 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.

Free Database

300,000+ Devices

4 Competitors

5 Recent Registrations

240002872/PCBB-HN

Registration Details

Vietnam MOH Registration: 240002872/PCBB-HN

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Magnesium Quantitative Testing Drug

VN: Thuốc thử xét nghiệm định lượng Magnesi

Risk Class TBYT Loại B

Registration Details

Analysis ID

240002872/PCBB-HN

Submission ID

000.00.19.H26-241004-0017

Product Type

MAGNESIUM

Product Code

OSR6189

Technical Details

Intended Use

Magnesium Test is an in vitro diagnostic medical device used by healthcare professionals to quantitate magnesium in human serum, plasma, and urine by the colorimetric method, using the Beckman Coulter AU/DxC AU automated analyzers. The measurement of magnesium is used in the diagnosis and treatment of hypomagnesemia (abnormally low) and hypermagnesemia (abnormally high).