| Primary Device ID | 00853023006104 |
| NIH Device Record Key | 82d9a30b-ca3d-41ab-9585-30b191603b78 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cerner Bridge Medical Transfusion Administration and Specimen Collections |
| Version Model Number | Bridge2016 |
| Company DUNS | 042410688 |
| Company Name | CERNER CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00853023006104 [Primary] |
| MMH | Software, Blood Bank, Stand Alone Products |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
| 00850017753112 - FetaLink+ | 2024-06-03 |
| 00850017753037 - Cerner Patient Observer | 2020-12-22 |
| 00853023006241 - Cerner Patient Observer | 2020-02-10 |
| 00853023006197 - Cerner Patient Observer | 2019-10-08 |
| 00853023006203 - Cerner Patient Observer | 2019-10-08 |
| 00853023006234 - Cerner Patient Observer | 2019-10-08 |
| 00853023006111 - Cerner CareAware Event Management | 2019-07-12 |
| 00853023006135 - Cerner CareAware Event Management | 2019-07-12 |