Urine
Multi-Panel
CE / IVDR
Certifies compliance with the European Union's In Vitro Diagnostic Medical Devices Regulation (IVDR 2017/746).
ISO 13485
International quality management system standard for medical device design and manufacturing.
ISO 9001
The foundational international standard for general quality management systems; ensures process consistency and customer satisfaction.
AB-PINACA (ABP) · UR-144 (UR-144) · Synthetic Marijuana (K2)
Product Code
CRT-MP12-U05
Number of Parameters
3 Parameters
Test Method
Immunochromatography
Result Time
5 minutes
Sample Type
Urine
Storage Conditions
2–30°C, away from direct sunlight
Shelf Life
24 months from production date
Test kit
Desiccant packet
User manual