| Entry No. | Guid | |
| Released | Boolean | |
| Internal Version | Integer | |
| Active | Boolean | |
| Transferred | Boolean | |
| Description | Text[100] | |
| Labeler DUNS Number | Integer | |
| Version or Model | Text[80] | |
| Catalog Number | Text[80] | |
| Device Description | Text[2000] | |
| Package DI | Text[120] | |
| Unit of Use DI | Text[120] | |
| Device Count | Integer | |
| Brand Name | Text[80] | |
| Primary DI Number | Text[120] | |
| DI Record Publish Date | Date | |
| CommercialDistributionEndDate | Date | |
| Issuing Entity Primary DI | Code[20] | |
| Issuing Entity Unit of Use DI | Code[20] | |
| Issuing Entity Package DI | Code[20] | |
| Iss. Entity Direct Marking DI | Code[20] | |
| Direct Marking DI | Text[120] | |
| DeviceSubjecttoDMbutExcepted | Boolean | |
| DMDIDifferentfromPrimaryDI | Boolean | |
| Issuing Entity Secondary DI | Code[20] | |
| Secondary DI | Text[120] | |
| Issuing Entity Previous DI | Code[20] | |
| Previous DI | Text[120] | |
| HumanCellTissueBasedProduct | Boolean | |
| Kit | Boolean | |
| CombinationProduct | Boolean | |
| DeviceExemptPremarketSubm | Boolean | |
| ForSingleUse | Boolean | |
| LotorBatchNumber | Boolean | |
| ManufacturingDate | Boolean | |
| SerialNumber | Boolean | |
| ExpirationDate | Boolean | |
| DonationIdentificationNumber | Boolean | |
| Devicerequiredlabelcontrubber | Boolean | |
| DeviceNotwithnaturallatex | Boolean | |
| PrescriptionUseRx | Boolean | |
| OvertheCounter | Boolean | |
| MRIsafetyinfolabelingcontain | Enum (KVSKBAUDIGUDIDMRSafety) | |
| DevicePackagedasSterile | Boolean | |
| RequiresSterilizationPriorUse | Boolean | |