| Primary Device ID | 00855141006417 |
| NIH Device Record Key | ea644b6a-19e1-4e1e-ac61-3d643c81b490 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MaximQA |
| Version Model Number | 1.0 |
| Company DUNS | 009120817 |
| Company Name | VARIAN MEDICAL SYSTEMS, INC. |
| 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 | true |
| 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 | 00855141006417 [Primary] |
| LHO | Instrument, Quality-Assurance, Radiologic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-03-12 |
| Device Publish Date | 2025-03-04 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MAXIMQA 97925937 not registered Live/Pending |
Varian Medical Systems, Inc. 2023-05-08 |