| Primary Device ID | 00840682144292 |
| NIH Device Record Key | fe57ce4e-2377-4ef1-8c0e-79c20dd79f2e |
| Commercial Distribution Discontinuation | 2025-06-04 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | CARESCAPE |
| Version Model Number | V100 |
| Company DUNS | 118935631 |
| 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 | 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 | 00840682144292 [Primary] |
| DQA | Oximeter |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-06-12 |
| Device Publish Date | 2025-06-04 |
| 00840682109833 | Central Station v1 upgrade |
| 00840682109826 | Central Station v1 |
| 00840682109383 | T14 Transmitter |
| 00840682109260 | Telemetry Server V4 |
| 00840682108775 | Telemetry Server v4 upgrade |
| 00840682103930 | 19 inch Display D19KT |
| 00840682103091 | V100 |
| 00840682144292 | V100 GENERIC ATO MODEL No CE |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CARESCAPE 77059764 3570349 Live/Registered |
General Electric Company 2006-12-08 |
![]() CARESCAPE 75619287 not registered Dead/Abandoned |
Reddy, Rama M. 1999-01-19 |
![]() CARESCAPE 75574654 2316008 Live/Registered |
Carescape, Inc. 1998-10-21 |