Rapid Tramadol Test (Strip)

Quality
Cut Off 100ng/ml
25
Kit Type

The Gold Medi Test Plus TML Urine Rapid Test is designed for the rapid and qualitative detection and identification of tramadol metabolites in urine. It is intended solely for forensic and in vitro diagnostic use.

This test operates based on the immunochromatography method and has a sensitivity of 100 ng/mL. This test is for rapid screening only and provides a preliminary result. A more specific alternative method should be used to confirm initial results; High-Performance Liquid Chromatography (HPLC) is the preferred method for this purpose. If the test result is positive, clinical examinations are necessary to determine substance abuse.

Product Description

The Rapid Tramadol Test (Strip) is designed for the rapid, qualitative detection of tramadol metabolites in urine. This test is performed using an immunochromatographic method and has a sensitivity of 100 ng/mL. Preliminary results must be confirmed by methods such as chromatography (HPLC).

Applications of the Rapid Tramadol Test (Strip)

This test is used for the rapid identification of tramadol use in medical, laboratory, and treatment screenings. It can also be used to detect tramadol abuse or misuse.

How to Use the Rapid Tramadol Test (Strip)

Keep the freshly collected urine sample at room temperature. Dip the test strip into the sample and examine the result within 5 minutes. The appearance of a line in the test region (T) indicates a negative result, while the absence of a line indicates a positive result. The control line (C) must always appear.

Precautions and Contraindications

  • This test is designed for in vitro diagnostic use only.
  • Positive results require confirmation with more precise methods.
  • Improper samples or incorrect usage conditions can lead to erroneous results.
  • Store the kit at 2 to 30 degrees Celsius, away from humidity and direct sunlight.
  • Avoid using expired, faulty, or previously used kits.
  • The test strip must be kept in its aluminum packaging until use. Use the test strip immediately upon opening the aluminum pouch.
  • Due to the infectious nature of all samples, adherence to hygiene protocols is essential.
  • Always interpret results under appropriate lighting conditions to prevent interpretation errors. Results read after 15 minutes are invalid.
  • If the aluminum pouch has been stored at 2 to 8 degrees Celsius (refrigerator temperature), allow it to sit at room temperature for at least 10 minutes before opening.
  • Additional clinical examinations are mandatory for the diagnosis of abuse or treatment.
Quality
Cut Off 100ng/ml
25
Kit Type

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