Khay thử xét nghiệm định tính kháng thể kháng H. pylori - Vietnam Registration 240003113/PCBB-HN
Access comprehensive regulatory information for Khay thử xét nghiệm định tính kháng thể kháng H. pylori 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 240003113/PCBB-HN and manufactured by Guangzhou Wondfo Biotech Co., Ltd.. The authorized representative in Vietnam is CÔNG TY TNHH AVANTA DIAGNOSTICS.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Medicon Company Limited, and 1 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.
Device Details
Registration Details
240003113/PCBB-HN
000.00.19.H26-241101-0007
Theo theo phụ lục
Theo phụ lục
Technical Details
One Step H. Pylori Serum/Plasma Test is a qualitative immunoassay test for the detection of H. pylori antibodies in serum or plasma, intended to support the diagnosis of H. pylori infection. It is intended for In-vitro diagnostic use at medical facilities only.
Dates and Status
Nov 14, 2024