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 |