| Primary Device ID | 04250668607233 |
| NIH Device Record Key | eb1e3a8a-76d7-4afe-8bdc-b1f28e97295a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ZEISS Mobile Centration |
| Version Model Number | 000000-2750-321 |
| Catalog Number | 000000-2750-321 |
| Company DUNS | 333928146 |
| Company Name | Carl Zeiss Vision GmbH |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04250668607233 [Primary] |
| HLG | Pupillometer, Ac-Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-01-23 |
| Device Publish Date | 2026-01-15 |
| 04250668607233 - ZEISS Mobile Centration | 2026-01-23 |
| 04250668607233 - ZEISS Mobile Centration | 2026-01-23 |
| 04250668606045 - VISUSCREEN 100 Compact | 2023-06-07 |
| 04250668606052 - VISUCORE 500 Refractor | 2023-06-07 |
| 04250668606717 - i.Terminal 2 | 2021-02-01 N/A |
| 04250668606618 - VISUCONSULT 500 | 2021-01-11 N/A |
| 04250668606625 - i.Profiler plus | 2021-01-11 N/A |
| 04250668606632 - ATLAS Review for i. Profiler plus | 2021-01-11 N/A |
| 04250668606649 - i.Terminal mobile | 2021-01-11 N/A |