Primary Device ID | 00812231034422 |
NIH Device Record Key | 687e127b-9419-4ecb-b5e0-25158f7d18db |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Omni |
Version Model Number | 83-10-5001 |
Company DUNS | 065016344 |
Company Name | SANTA BARBARA IMAGING SYSTEMS, INC. |
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 | 805-770-2110 |
info@sbimagingsystems.com | |
Phone | 805-770-2110 |
info@sbimagingsystems.com | |
Phone | 805-770-2110 |
info@sbimagingsystems.com | |
Phone | 805-770-2110 |
info@sbimagingsystems.com | |
Phone | 805-770-2110 |
info@sbimagingsystems.com | |
Phone | 805-770-2110 |
info@sbimagingsystems.com | |
Phone | 805-770-2110 |
info@sbimagingsystems.com | |
Phone | 805-770-2110 |
info@sbimagingsystems.com | |
Phone | 805-770-2110 |
info@sbimagingsystems.com | |
Phone | 805-770-2110 |
info@sbimagingsystems.com | |
Phone | 805-770-2110 |
info@sbimagingsystems.com | |
Phone | 805-770-2110 |
info@sbimagingsystems.com | |
Phone | 805-770-2110 |
info@sbimagingsystems.com | |
Phone | 805-770-2110 |
info@sbimagingsystems.com | |
Phone | 805-770-2110 |
info@sbimagingsystems.com | |
Phone | 805-770-2110 |
info@sbimagingsystems.com | |
Phone | 805-770-2110 |
info@sbimagingsystems.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00812231034415 [Primary] |
GS1 | 00812231034422 [Package] Contains: 00812231034415 Package: 83-10-5001-RM [1 Units] In Commercial Distribution |
GCJ | Laparoscope, General & Plastic Surgery |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-07-02 |
Device Publish Date | 2024-06-24 |
00812231032978 | 4K UHD CAMERA HEAD, INTEGRATED, 1CMOS, HOLOGIC |
00812231032831 | TABLET, HOLOGIC |
00812231032961 | 4K UHD CAMERA CONTROL UNIT |
00812231032923 | ACMI LIGHT GUIDE POST ADAPTER |
00812231032916 | STORZ LIGHT GUIDE POST ADAPTER |
00812231032909 | WOLF LIGHT GUIDE POST ADAPTER |
00812231032893 | 5MM LIGHT GUIDE, BLUE |
00812231032886 | 5MM LIGHT GUIDE, GREY |
00812231032947 | CAMERA HEAD TRAY, HOLOGIC |
00812231033531 | 4K UHD CAMERA CONTROL UNIT, HOLOGIC, JPN |
00812231033524 | Tablet, Hologic, JPN |
00812231034453 | OMNI 4K HDR SYSTEM, TABLET |
00812231034446 | OMNI 4K HDR SYSTEM, CAMERA HEAD, INTEGRATED, 1C |
00812231034422 | OMNI 4K HDR SYSTEM, CAMERA CONTROL UNIT WITH IMAGE CAPTURE & LIGHT ENGINE |
00812231033470 | OMNI 4K HDR SYSTEM, TABLET, TETHERED |
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 |