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Khay thử xét nghiệm định tính kháng nguyên H.pylori - Vietnam Registration 220000825/PCBB-HCM

Access comprehensive regulatory information for Khay thử xét nghiệm định tính kháng nguyên H.pylori 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 220000825/PCBB-HCM and manufactured by Diagnosis F Biotech Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Asan Pharmaceutical Co., Ltd., Abbott Diagnostics Korea Inc., 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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220000825/PCBB-HCM
Registration Details
Vietnam MOH Registration: 220000825/PCBB-HCM
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Device Details

Khay thử xét nghiệm định tính kháng nguyên H.pylori
dfu EASY TEST H.pylori Ag
Risk Class TTBYT Loại B

Registration Details

220000825/PCBB-HCM

000.00.19.H29-220225-0028

dfu EASY TEST H.pylori Ag

H19

Company Information

Technical Details

Qualitative detection of Helicobacter pylori antigen in human stool sample

Dates and Status

Mar 17, 2022