| Primary Device ID | 10610586036606 |
| NIH Device Record Key | 7d931400-2867-4760-b880-79246996d18f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BCI |
| Version Model Number | 6004006 |
| Company DUNS | 118380146 |
| Company Name | ICU MEDICAL, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| 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 | 10610586036606 [Primary] |
| DXN | SYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2025-04-16 |
| Device Publish Date | 2016-10-13 |
| 10610586040689 | 21-0470-0105-24 |
| 10610586038334 | 6120LA |
| 10610586038143 | 9212A |
| 10610586038099 | 92M774325A |
| 10610586038082 | 92M774325 |
| 10610586037399 | 920654335A |
| 10610586037368 | 920654235A |
| 10610586037344 | 920654230A |
| 10610586037313 | 920654220A |
| 10610586036873 | 9004051 |
| 10610586036866 | 9004050 |
| 10610586036859 | 9004007 |
| 10610586036842 | 9004005 |
| 10610586036835 | 9004002 |
| 10610586036828 | 9004001 |
| 10610586036811 | 9004000 |
| 10610586036736 | 8400D |
| 10610586036606 | 6004006 |
| 10610586036590 | 6004004 |
| 10610586036583 | 6004001 |
| 10610586036576 | 6004000 |
| 10610586036521 | 3304LS |
| 10610586036415 | 9004003 |
| 10610586036378 | 9212S |
| 08426638170687 | 6120N |
| 08426638170663 | 6120SA |
| 08426638170656 | 6120C |
| 08426638170649 | 6120SC |
| 08426638163108 | 6120A |