Rapid Combo Test

Gamma-Hydroxybutyric Acid/Ketamine Combo Rapid Test (GHB/KET)

Simultaneous detection of GHB and Ketamine in urine.

CE Certified
ISO 13485
Main image of Gamma-Hydroxybutyric Acid/Ketamine Combo Rapid Test (GHB/KET)

Why Choose reOpenTest Toxicology & Drug Monitoring Kits?

Our tests are engineered for accuracy, reliability, and ease of use, ensuring confidence in every result.

Dual Detection

Simultaneously detects GHB and Ketamine for comprehensive screening.

Rapid Results

Provides presumptive results within minutes for quick decision-making.

Professional Use

Intended for clinical and forensic settings, aiding informed decisions.

Product Overview

The Gamma-Hydroxybutyric Acid/Ketamine Combo Rapid Test (GHB/KET) is an immunochromatography based one step in vitro test. It is designed for qualitative determination of Gamma-Hydroxybutyric acid (GHB) and Ketamine in human urine specimens.

Technical Specifications

Detection Target GHB and Ketamine
Sample Type Urine
Methodology Immunochromatography
Detection Range Qualitative (Positive/Negative)
Reaction Time 10-15 minutes
Storage Conditions 2-30u00b0C
Shelf Life 24 months

Procedure & Interpretation

Step-by-Step Procedure

  1. Collect urine sample in a clean, dry container.
  2. Dip the test strip into the urine sample for the specified time.
  3. Read the results within 10-15 minutes.

Result Interpretation

Positive Result
Positive: A visible colored line in the control region (C) and no line in the test region (T) indicates a positive result.
Negative Result
Negative: A visible colored line in both the control region (C) and the test region (T) indicates a negative result.
Invalid Result
Invalid: If no line appears in the control region (C), the test is invalid and should be repeated.

Frequently Asked Questions

The cutoff concentrations are specific to each drug and are detailed in the product insert.

No, this is a qualitative test providing only positive or negative results. For quantitative analysis, a more sophisticated laboratory method is required.

While the test is highly specific, certain interfering substances or medications could potentially cause a false positive. Refer to the product insert for a list of known interferents.

Technical Documents

Download product inserts and brochures for detailed information.

No technical documents are available at this time. Please check back soon.

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