Khay thử xét nghiệm định tính kháng nguyên Dengue NS1 - Vietnam Registration 2403582ĐKLH/BYT-HTTB

Access comprehensive regulatory information for Khay thử xét nghiệm định tính kháng nguyên Dengue NS1 in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại C medical device is registered under number 2403582ĐKLH/BYT-HTTB and manufactured by HUMASIS CO., LTD.. The authorized representative in Vietnam is CÔNG TY TNHH HUMASIS VINA.

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including Asan Pharmaceutical Co., Ltd., Medicon Company Limited, 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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2403582ĐKLH/BYT-HTTB

Registration Details

Vietnam MOH Registration: 2403582ĐKLH/BYT-HTTB

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Device Details

Khay thử xét nghiệm định tính kháng nguyên Dengue NS1

Humasis Dengue NS1 Antigen Test

Risk Class TTBYT Loại C

Registration Details

Analysis ID

2403582ĐKLH/BYT-HTTB

Submission ID

000.00.04.G18-230912-0012

Product Type

Theo theo phụ lục

Product Code

Theo phụ lục

Technical Details

Intended Use

Humasis Dengue NS1 Antigen Test is an in vitro diagnostic test device based on the immuno-precipitation method, designed to qualitatively detect the Dengue NS1 antigen in blood and plasma/serum.