| Primary Device ID | 00840682140744 |
| NIH Device Record Key | 26cd3a64-a401-4208-bbe4-ffe21ba59250 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ViewPoint |
| Version Model Number | 6. ver10 |
| Company DUNS | 507406770 |
| Company Name | GE Healthcare GmbH |
| 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 | 00840682140744 [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 | 3 |
| Public Version Date | 2019-05-23 |
| Device Publish Date | 2018-08-14 |
| 00840682145718 | 6. ver11 |
| 00840682140744 | 6. ver10 |
| 00840682124454 | 6. ver6.9 |
| 00840682119627 | 6 ver6.8 |
| 00840682119610 | ver5.6 |
| 00840682103640 | 6 ver 6.7 |
| 00840682171953 | 6. ver12 |
| 00195278517340 | ViewPoint 6 v6.14 |
| 00195278753472 | ViewPoint 6 v6.15 |