Rapid drug detection test GD-QCY-0005

for ecstasyurineimmunochromatographic

Product Overview
Xenta Methylenedioxymethamphetamine (MDMA) rapid test kit is an in vitro diagnostic device based on a gold immunochromatographic assay for the qualitative detection of methylenedioxymethamphetamine (MDMA) in human urine.

Key Product Information
Product Name: Methylenedioxymethamphetamine (MDMA) Rapid Test Kit
Catalog No.: GD-QCY-0005
Brand: Xenta
Certification: FDA
Analyte: Methylenedioxymethamphetamine (MDMA)
Complexity: Moderate
Sample Type: Urine
Validation Methods: GC-MS
Test Time: 5 min (read at 5 minutes; do not interpret after 10 minutes)
Test Temperature: 15-30°C
Storage: Store at 2-30°C
Application: In vitro qualitative screening for MDMA in human urine.

Quantities and Packaging
Available configuration: 10 tests per kit.

Test Procedure (Operations)

• Collect urine specimen in a clean urine cup.
• Open the sealed pouch and remove the test device. Place on a level surface.
• Using the provided dropper, add exactly three drops of urine into the sample well.
• Read the result at 5 minutes. Do not interpret results after 10 minutes.

Notes
For in vitro diagnostic use only. Follow local regulations and institutional protocols for specimen handling and disposal.

Technical specifications

• Analyte: Methylenedioxymethamphetamine (MDMA)
• Sample Type: Urine
• Test Principle: Gold immunochromatographic assay
• Validation Method: GC-MS
• Test Time: 5 minutes (read at 5 min; do not interpret after 10 min)
• Operating Temperature: 15-30°C
• Storage Conditions: 2-30°C
• Complexity: Moderate
• Compatible Test Tools: Drug screen cup, drug screen dipcard
• Certification: FDA