| Primary Device ID | 00840682139267 |
| NIH Device Record Key | 0e839692-8814-4dea-800a-1ae15a053314 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Brivo |
| Version Model Number | NM 615 |
| Company DUNS | 654659689 |
| Company Name | Hangwei GE Medical Systems Co., Ltd. |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840682139267 [Primary] |
| KPS | System, tomography, computed, emission |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-09-21 |
| Device Publish Date | 2018-08-21 |
| 00840682139267 | NM 615 |
| 00840682118149 | XR385 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BRIVO 77539010 4150409 Live/Registered |
General Electric Company 2008-08-05 |
![]() BRIVO 77267496 3439769 Dead/Cancelled |
Brivo LLC 2007-08-29 |
![]() BRIVO 76237266 2540211 Live/Registered |
BRIVO SYSTEMS, LLC 2001-04-09 |
![]() BRIVO 76237265 2558582 Live/Registered |
BRIVO SYSTEMS, LLC 2001-04-09 |
![]() BRIVO 76237264 2529781 Live/Registered |
BRIVO SYSTEMS, LLC 2001-04-09 |
![]() BRIVO 76049941 2724876 Dead/Cancelled |
BRIVO SYSTEMS, LLC 2000-05-17 |
![]() BRIVO 76049940 not registered Dead/Abandoned |
BRIVO SYSTEMS, INC. 2000-05-17 |
![]() BRIVO 76049931 2689042 Dead/Cancelled |
BRIVO SYSTEMS, LLC 2000-05-17 |