| 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 |
| 00198953061329 - NMCT 860 | 2025-09-17 NM_CT 860 NM Gantry Final MDR |
| 00198953061336 - NMCT 850 | 2025-09-17 NM_CT 850 NM Gantry Final MDR |
| 00195278878502 - Aurora | 2025-03-05 AURORA NM GANTRY FINAL |
| 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 |
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 |