| Primary Device ID | 00840682144803 |
| NIH Device Record Key | 2bef94a8-371c-43d1-818a-5c083d1b963f |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 2059291-501 |
| Catalog Number | 2059291-001 |
| Company DUNS | 006580799 |
| Company Name | GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, 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 | 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 | 00840682119979 [Package] Package: [10 Units] In Commercial Distribution |
| GS1 | 00840682144803 [Primary] |
| DXQ | Blood Pressure Cuff |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-05-09 |
| Device Publish Date | 2025-05-01 |
| 00840682144803 - NA | 2025-05-09Y-ADAPTER 1 TB BAYONET MALE TO 2 TB 80369-5 DINACLICK FEM, SINGLE |
| 00840682144803 - NA | 2025-05-09 Y-ADAPTER 1 TB BAYONET MALE TO 2 TB 80369-5 DINACLICK FEM, SINGLE |
| 00840682118910 - NA | 2025-05-02 Y-ADAPTER 1 TB BAYONET MALE TO 2 TB DINACLICK FEM, SINGLE |
| 00840682188968 - MLCL Upgrade | 2025-04-21 Upgrade Kit MLCL V7.1 |
| 00840682124669 - NA | 2025-04-18 ASSY CARESCAPE ONE NIBP HOSE NEONATAL 2T NEO-SNAP 2.4M |
| 00840682124683 - NA | 2025-04-18 ASSY CARESCAPE ONE NIBP HOSE NEONATAL 2T NEO-SNAP 3.6M |
| 00195278421449 - CAM | 2025-04-15 CAM 14 - MDR |
| 00195278421456 - CAM | 2025-04-15 CAM HD - MDR |
| 00195278364661 - CardioSoft | 2025-04-02 CARDIOSOFT V7.0 SP7.2 |