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 |