Primary Device ID | 07290016746716 |
NIH Device Record Key | 8e244202-3b4f-4fc2-8f32-2346d3b5f0f0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Console |
Version Model Number | MM40000-US |
Catalog Number | MM40000-US |
Company DUNS | 514612758 |
Company Name | VIORA 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 |
Phone | 888 415 1192 |
CustomerCareUsa@sinclair.com | |
Phone | 888 415 1192 |
CustomerCareUsa@sinclair.com | |
Phone | 888 415 1192 |
CustomerCareUsa@sinclair.com | |
Phone | 888 415 1192 |
CustomerCareUsa@sinclair.com | |
Phone | 888 415 1192 |
CustomerCareUsa@sinclair.com | |
Phone | 888 415 1192 |
CustomerCareUsa@sinclair.com | |
Phone | 888 415 1192 |
CustomerCareUsa@sinclair.com | |
Phone | 888 415 1192 |
CustomerCareUsa@sinclair.com | |
Phone | 888 415 1192 |
CustomerCareUsa@sinclair.com | |
Phone | 888 415 1192 |
CustomerCareUsa@sinclair.com | |
Phone | 888 415 1192 |
CustomerCareUsa@sinclair.com | |
Phone | 888 415 1192 |
CustomerCareUsa@sinclair.com | |
Phone | 888 415 1192 |
CustomerCareUsa@sinclair.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07290016746716 [Primary] |
KZE | Injector, Fluid, Non-Electrically Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2025-07-31 |
Device Publish Date | 2025-05-22 |
07290016746716 - Console | 2025-07-31EnerJet Console |
07290016746716 - Console | 2025-07-31 EnerJet Console |
07290016746723 - Applicator | 2025-07-31 EnerJet Applicator |
07290016746730 - Trolley | 2025-07-31 EnerJet Trolley |
07290016746747 - Disposable Delivery Nozzle | 2025-07-31 EnerJet Delivery Nozzle |
07290016746761 - Treatment Kit 2.0 | 2025-07-31 EnerJet Treatment Kit |
07290016746440 - ST Single Use Tip | 2025-06-30 ST Single Use Tip |
07290016746495 - DermaFuse | 2025-05-29 DermaFuse console |
07290016746679 - Brush Single-Use Tip | 2025-05-29 Brush Single-Use Tip for use with Dermafuse |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() CONSOLE 97638120 not registered Live/Pending |
Console Ltd. 2022-10-19 |
![]() CONSOLE 97414514 not registered Live/Pending |
Veriti Management LLC 2022-05-17 |
![]() CONSOLE 90609125 not registered Live/Pending |
Console Ltd 2021-03-29 |
![]() CONSOLE 90609123 not registered Live/Pending |
Console Ltd 2021-03-29 |
![]() CONSOLE 86723435 5093696 Live/Registered |
PCCW-HKT DATACOM SERVICES LIMITED 2015-08-13 |
![]() CONSOLE 86485001 4781980 Live/Registered |
AppNexus Inc. 2014-12-18 |
![]() CONSOLE 85164683 not registered Dead/Abandoned |
Orpyx Medical Technologies Inc. 2010-10-29 |
![]() CONSOLE 78765576 not registered Dead/Abandoned |
Bioniche Life Sciences Inc. 2005-12-02 |
![]() CONSOLE 77136316 3477495 Dead/Cancelled |
Falcon Footwear, Inc. 2007-03-21 |
![]() CONSOLE 76663868 3468464 Live/Registered |
CLEARONE, INC. 2006-07-31 |
![]() CONSOLE 76571709 3130291 Dead/Cancelled |
Performance Assessment Network, Inc. 2004-01-23 |
![]() CONSOLE 74714665 2109567 Dead/Cancelled |
HUNTLEIGH TECHNOLOGY LIMITED 1995-08-14 |