| Primary Device ID | 00840682145794 |
| NIH Device Record Key | 907ae722-ee6a-45bb-bd37-76b641fc3e70 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CENTRICITY |
| Version Model Number | UNIVERSAL VIEWER 7.0 |
| Company DUNS | 054324257 |
| Company Name | GE HEALTHCARE |
| 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 | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)437-1171 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840682145794 [Primary] |
| LLZ | System, image processing, radiological |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2020-02-04 |
| Device Publish Date | 2020-01-17 |
| 00840682104821 | CPACS RA1000 6.0 |
| 00840682145794 | UNIVERSAL VIEWER 7.0 |
| 00840682145572 | CPACS 7.0 |
| 00840682141642 | Perinatal 6.98 |
| 00840682124430 | CPACS 4.0 |
| 00840682123785 | Perinatal6.97 |
| 00840682104807 | CPACS 6.0 |
| 00840682103800 | UNIVERSAL VIEWER 6.0 |
| 00840682102988 | UNIVERSAL VIEWER ZFP CLIENT 6.0 |
| 00840682102681 | PERINATAL6.96 |
| 00840682145558 | CPACS 7.0 |
| 00840682124447 | MD CPACS RA1000 4.0 MEDICAL DEVICE |