| 104926-1 | Device manufacture date |
| 104927-9 | Catalog number |
| 104985-7 | Resource identifier for device Narrative |
| 107097-8 | Medical device description Narrative |
| 111763-9 | Sampling frequency |
| 111764-7 | Sampling context Narrative |
| 44615-3 | Device error code |
| 63518-5 | DXA instrument make and model name |
| 67099-2 | Vendor device name |
| 67715-3 | Vendor device model type |
| 67716-1 | Vendor device model |
| 74700-6 | Ergonomics or human AndOr device interface issue |
| 74701-4 | Problem that resulted from the equipment or device function problem |
| 74702-2 | Circumstances involving the health information technology device in the event or unsafe condition |
| 74705-5 | Best characterization of health information technology (HIT) device |
| 74710-5 | Asset tag number |
| 74711-3 | Unique device identifier |
| 74712-1 | Expiration date |
| 74713-9 | Other unique product identifier |
| 74714-7 | Lot or batch number |
| 74715-4 | Vendor serial number |
| 74716-2 | Vendor firmware version |
| 74717-0 | Vendor model number |
| 74718-8 | Type of device identifier |
| 74719-6 | Manufacturer name |
| 74720-4 | Device name |
| 74723-8 | Device involved in patient safety event or unsafe condition |
| 74726-1 | Other unique product identifier |
| 82307-0 | Vendor device information panel |
| 88662-2 | Defibrillator type |
| 88664-8 | Mode of defibrillation |
| 89203-4 | Airway suction device |
| 90370-8 | LIVD mapping data set |
| 91604-9 | Device count |
| 92038-9 | Information communication technology type |
| 92039-7 | Information communication technology name |
| 92040-5 | Information communication technology description |
| 92192-4 | Equipment type available |
| 95293-7 | Device measurement mode |