| 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 |
|
| Storage Handling Conditions |
Boolean |
|