| Primary Device ID | 00195278798374 | 
| NIH Device Record Key | afb25c68-a4ae-4107-b56d-60f4fda85f23 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | AMX | 
| Version Model Number | NAVIGATE UPGRADE | 
| Company DUNS | 809785715 | 
| Company Name | GE MEDICAL SYSTEMS, INC. | 
| 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 | false | 
| Serial Number | true | 
| 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 | 
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00195278798374 [Primary] | 
| IZL | System, x-ray, mobile | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2024-02-01 | 
| Device Publish Date | 2024-01-24 | 
| 00195278003348 | AMX Navigate Designated Medical Device Assembly | 
| 00195278798374 | AMX Navigate Upgrade Designated Medical Device Assembly |