| Primary Device ID | 00840682103251 |
| NIH Device Record Key | e64466f6-420b-4ce3-b16c-3ae3b5d9d04a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TruSignal SpO2 |
| Version Model Number | TS-E-D |
| Company DUNS | 401966697 |
| Company Name | GE Healthcare Finland Oy |
| 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 | 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 | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)558-5120 |
| xx@xx.xx |
| Storage Environment Temperature | Between -40 Degrees Celsius and 60 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840682103251 [Primary] |
| DQA | Oximeter |
| 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 | 2016-06-16 |
| 00840682103435 | TS-F4-GE |
| 00840682103428 | TS-E4-GE |
| 00840682103411 | TS-SP3-GE |
| 00840682103404 | TS-SP-D |
| 00840682103398 | TS-N3 |
| 00840682103381 | TS-E4-N |
| 00840682103367 | TS-E4-H |
| 00840682103343 | TS-F1-H |
| 00840682103329 | TS-SA-D |
| 00840682103312 | TS-G3 |
| 00840682116695 | TS-AAW |
| 00840682103282 | TS-SE-3 |
| 00840682116725 | TS-PAW |
| 00840682103251 | TS-E-D |
| 00840682103244 | TS-H3 |
| 00840682103237 | TS-SA4-GE |
| 00840682116770 | TS-AP |
| 00840682103206 | TS-F-D |
| 00840682103190 | TS-F4-N |
| 00840682116749 | TS-AF |
| 00840682103169 | TS-F4-MC |
| 00840682103152 | TS-F2-GE |
| 00840682103138 | TS-E2-GE |
| 00840682103121 | TS-W-D |
| 00840682103114 | TS-M3 |