QZH

Opioid Use Disorder Genetic Risk Variant Detection System And Collection Kit

Product code

QZH

Device name

Opioid Use Disorder Genetic Risk Variant Detection System And Collection Kit

Device class

Class 3

Medical specialty

Unknown

Marketing pathway

PMA

FDA classification definition

A qualitative in vitro molecular test that detects select variants in genomic DNA isolated from human specimens. Results of the test provide users with a genetic risk assessment of developing Opioid Use Disorder (OUD) and are intended to aid users with informed decision-making regarding the use of oral opioids for acute pain relief. The test may not include all variants associated with a risk of developing OUD and is not intended to describe a person’s overall risk of developing OUD. Results from the system are intended to be used in combination with clinical information and should not be the sole determinant in diagnosing, counseling, or making prescribing decisions

Definition text from the FDA device classification database (U.S. federal government work, public domain).