Primary Device ID | 08426638170649 |
NIH Device Record Key | 5e8a9095-8192-499a-8ea3-528f5f6b3870 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BCI |
Version Model Number | 6120SC |
Company DUNS | 118380146 |
Company Name | ICU MEDICAL, INC. |
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 | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08426638170649 [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 | 2016-11-16 |
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 |