Auxiliary Diagnosis · Medical diagnostics

Acute myocardial infarction auxiliary diagnosis kit

IVD reagent product positioned for auxiliary diagnosis of acute myocardial infarction by detecting H-FABP in human urine.

Acute myocardial infarction auxiliary diagnosis kit product visual for H-FABP IVD rapid test kit

Product Description

An IVD reagent product positioned for auxiliary diagnosis of acute myocardial infarction by detecting H-FABP in human urine.

It is intended for medical institution use and should be interpreted together with clinical symptoms, ECG and other laboratory indicators.

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Product Information

Product Type
IVD reagent product
Marker
H-FABP in human urine
Purpose
Auxiliary diagnosis support for acute myocardial infarction
User
Medical institutions
Compliance
Subject to local registration and clinical application rules

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.

Clinical Auxiliary Reference

The brochure emphasizes early rapid detection as support for clinical decision-making.
This product should not be used as the sole basis for diagnosis or treatment decisions.
Local medical device registration, import approval and advertising requirements should be verified before distribution.

Applicable Medical 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

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.

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