| Name | Value |
|---|---|
| SERVICE REASON CODE | DI |
| BRIEF DESCRIPTION | Device Identifier |
| CODE TYPE ABBREVIATION | CIQ |
| CODE DESCRIPTION | COMPOUND INGREDIENT PRODUCT CODE QUALIFIER |
| FULL DESCRIPTION | Mandatory, fixed portion of a Unique Device Identifier (UDI) that identifies the specific version or model of a device and the labeler of that device. The DI portion is issued by Federal Drug Administration (FDA) Accredited Issuing Agencies such as GS1 and HIBCC. |