UniqueDeviceIdentifierCategory Class |
| Name | Type | Description | |
|---|---|---|---|
| Area | string |
Area where the device was implanted
|
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| Brand | string |
The device's brand name
|
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| Category | string |
The category name ("UniqueDeviceIdentifier")
|
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| Company | string |
The device's company name
|
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| Description | string |
The device's description
|
|
| DiscoveryDate | dateTime |
Discovery date
|
|
| DistinctId | string |
Identification code for a human cell, tissue, or
cellular and tissue-based product (HCT/P) regulated
as a device
|
|
| ExpirationDate | dateTime |
The device's expiration date
|
|
| GmdnPtName | string |
Association with the Device Identifier in the Global
Unique Device Identification Database (GUDID).
|
|
| Labeled | string |
Whether the UDI is labeled as containing NRL
|
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| Lot | string |
Lot or batch number within which a device was manufactured
|
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| ManufacturingDate | dateTime |
The device's manufacturing date
|
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| MRISafetyStatus | string |
The device's MRI safety status
|
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| Notes | string |
Notes
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| SerialNumber | string |
The device's serial number
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| Status | string |
The device's status
|
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| UDI | string |
Unique device identifier
|
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| VersionModelNumber | string |
The device's version model number
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