IVD Rapid TestPOCT Channel

Shanghai Yijun Medical Technology — YIJUN H-FABP Rapid Test Kit

A urine-based H-FABP rapid test kit designed for in-vitro qualitative detection of heart-type fatty acid-binding protein in human urine, supporting auxiliary diagnosis of acute myocardial infarction in medical institutions.

IVD product showcase + acute myocardial infarction auxiliary testing page + medical channel cooperation inquiry page.

Shanghai Yijun Medical Technology Co., Ltd. YIJUN H-FABP rapid test kit poster for medical diagnostics
Shanghai Yijun Medical Technology Co., Ltd. H-FABP rapid test rollup banner and product highlightsShanghai Yijun Medical Technology Co., Ltd. H-FABP test kit instruction and product package

Product Overview

YIJUN H-FABP Rapid Test Kit is an in-vitro diagnostic reagent kit for detecting heart-type fatty acid-binding protein in human urine.

According to the promotional materials, H-FABP is rapidly released after myocardial injury and can be detected in urine. The product is positioned as a non-invasive, convenient and rapid auxiliary testing tool for medical institutions.

Shanghai Yijun Medical Technology Co., Ltd. H-FABP rapid test kit product overview and use instruction

Key Product Advantages

Urine-based testing
Non-invasive sampling
Rapid response
Simple operation
Clinical auxiliary reference
Early indication support
Sensitive monitoring
Suitable for medical institutions
Designed for H-FABP qualitative detection
Supports acute myocardial infarction auxiliary diagnosis

H-FABP Marker Explanation

H-FABP stands for heart-type fatty acid-binding protein. It is described in the brochure as a protein rich in myocardial tissue and as a potential early marker for myocardial injury.

The brochure explains that H-FABP has small molecular size and can be detected within approximately 3 hours after myocardial injury, making it a reference marker for early myocardial injury evaluation.

Shanghai Yijun Medical Technology Co., Ltd. H-FABP marker explanation and clinical reference material

Market & Clinical Need

The brochure states that acute myocardial infarction deaths in China exceed 1.3 million cases per year, with an annual growth rate of 7.8%. It also highlights that early diagnosis still has unmet clinical needs.

The material emphasizes that time is life for AMI, and early rapid detection can help support clinical decision-making.

Testing Method

Method 1: drop urine sample into the sample well and read the result after standing for 5-15 minutes.
Method 2: collect urine with a disposable urine cup, insert the test strip into the urine sample, and read the result after 5-15 minutes.
Result interpretation includes positive, negative and invalid result examples.
Shanghai Yijun Medical Technology Co., Ltd. urine H-FABP rapid test method and result interpretation

Registration & Compliance Information

The promotional materials display Chinese medical device registration information and product registration certificate content.

The page presents the product as an IVD test kit for medical institutions and avoids exaggerated claims. Market access, registration, import approval and clinical application requirements may vary by country or region.

Shanghai Yijun Medical Technology Co., Ltd. Chinese medical device registration and product certificate material

Product & Technology Pages

Application Scenarios

Hospitals
Emergency departments
Clinics
Medical laboratories
Physical examination centers
Primary healthcare institutions
POCT testing scenarios
Medical device distributors
IVD product channels
Acute myocardial infarction auxiliary testing
Myocardial injury marker monitoring

Cooperation Models

Medical device distribution
IVD reagent channel cooperation
Hospital and clinic supply
POCT product cooperation
Regional agency cooperation
OEM / ODM discussion
Public health project supply
Medical laboratory cooperation
Import registration cooperation
Product catalog cooperation
Training and after-sales support

Compliance Notice

The information on this page is for business introduction, product distribution discussion and market cooperation only. This product is an in-vitro diagnostic product for medical institution use. It should not be used as the sole basis for diagnosis or treatment decisions. Clinical interpretation should be combined with symptoms, ECG and other laboratory indicators. Product registration, import approval, advertising claims and clinical application requirements may vary by country or region. Partners should verify local regulations before distribution or promotion.