UDID
The following table shows UDID attributes
| Attribute | Description |
|---|---|
| GUDID | The unique identifier for Global Unique Device Identification Database. |
| Brand Name | The name of the brand. |
| Catalog Number | The number of the catalog. |
| Commercial Distribute End Date | The end date of the commercial distribution. |
| Commercial Distribute Status | The status of the commercial distribution. |
| Company Name | The name of the company. |
| Contains DI Number | This contains the DI Number. |
| Device Combination Product | This is the product combination. |
| Device Count | The device count. |
| Device Description | The device description. |
| Device HCTP | The Human Cell Tissue or Cellular or TissueBased Product (HCT/P). |
| Device Kit | The device kit. |
| Device Packaged as Sterile | The Sterile Device. |
| Device Record Status | The device record status. |
| Device Type | The device type. |
| DI Record Publish Date | The DI record publish date. |
| DME Exempt | The device subject to Direct Marking (DM), but also exempt. |
| Donation ID Number | The donation identification number. |
| The manufacturer’s email address. | |
| Expiration Date | The date of expiration. |
| GUDID URL | The GUDID URL. |
| Issuing Agency | The issuing agency. |
| Labeled Contains No-NRL | The device labeled not made with natural rubber latex. |
| Labeled Contains NRL | The device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437). |
| Log Batch | The lot or batch number. |
| Manufacturer Date | The manufacturing date. |
| OTC | Over the Counter (OTC). |
| Package DI Number | The Package DI Number. |
| Phone | A manufacturer’s phone number. |
| Pre-Market Exempt | Defines whether something is Pre-Market Exempt or not. |
| Prescription Use (Rx) | Defines whether something is the Prescription Use (Rx) or not. |
| Primary DI Number | This contains the Primary DI Number. |
| Quantity Per Package | The quantity per package. |
| Requires Sterilization Prior to Use | This requires sterilization prior to use. |
| Serial Number | The serial number. |
| Single Use | For Single-Use. |
| Sterilization Method | The sterilization method. |
| Unit Of Use DI Number | The unit of use DI Number. |
| Version or Model | The version or model. |
| MRI Safety Status | What MRI safety information the labeling contains. |
| Is Private? | Yes = Private entry; No = Original Technopedia entry |
| Private Flag | 0 = Not Modified (i.e. original Technopedia entry); 1 = Modified Technopedia object; 2 = Proprietary object (those that have negative IDs). |
| Private Type | PRIVATE_TYPE = NULL if PRIVATE_FLAG = 0,PRIVATE_TYPE = Modified Technopedia entry if PRIVATE_FLAG = 1,PRIVATE_TYPE = Proprietary entry if PRIVATE_FLAG = 2. |