Primary Device ID | 00195278592309 |
NIH Device Record Key | 50a3af3c-54ef-4706-bbc4-1b6a1d9e5b81 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Omni |
Version Model Number | Legend |
Company DUNS | 532102365 |
Company Name | G E MEDICAL SYSTEMS ISRAEL 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 | true |
Serial Number | true |
Manufacturing Date | false |
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 |
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 | 00195278592309 [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 | 2022-09-20 |
Device Publish Date | 2022-09-12 |
00195278870490 - StarGuide MDD to MDR Upgrade | 2024-05-24 StarGuide SW and Labels Upgrade |
00195278755544 - StarGuide | 2024-04-26 StarGuide NM GANTRY MDR FINAL |
00195278794772 - D630 to D670 DR Upgrade | 2024-03-26 D630 to D670 DR NM GANTRY UPGRADE KIT |
00195278788252 - NM | 2023-11-23 830 NM GANTRY FINAL WITH NEW ROTOR - MDR CE |
00195278788269 - NMCT | 2023-11-22 870 DR NM GANTRY FINAL WITH NEW ROTOR - MDR CE |
00195278488619 - MyoSPECT | 2023-09-22 MyoSPECT MDR GANTRY |
00195278488626 - MyoSPECT ES | 2023-09-22 MyoSPECT ES MDR GANTRY |
00195278722546 - MyoSEPCT ES to MyoSPECT Upgrade | 2023-09-22 MyoSPECT ES to MyoSPECT Upgrade kit |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
OMNI 98888741 not registered Live/Pending |
British American Tobacco (Brands) Limited 2024-12-06 |
OMNI 98768534 not registered Live/Pending |
OmniMetrix, LLC 2024-09-25 |
OMNI 98611364 not registered Live/Pending |
Gravity Brands Limited 2024-06-20 |
OMNI 98504606 not registered Live/Pending |
OmniOrder 2024-04-17 |
OMNI 98408810 not registered Live/Pending |
Canby Telephone Association 2024-02-16 |
OMNI 98408809 not registered Live/Pending |
Canby Telephone Association 2024-02-16 |
OMNI 98382458 not registered Live/Pending |
Universal Instruments Corporation 2024-01-30 |
OMNI 98374513 not registered Live/Pending |
Tractian LLC 2024-01-24 |
OMNI 98323987 not registered Live/Pending |
IVISION TECH INC. 2023-12-20 |
OMNI 98294861 not registered Live/Pending |
IVISION TECH, Inc. 2023-12-01 |
OMNI 98292411 not registered Live/Pending |
ChargePoint, Inc. 2023-11-30 |
OMNI 98291159 not registered Live/Pending |
Remarc Vending, LLC 2023-11-29 |