| Primary Device ID | 00889095048186 |
| NIH Device Record Key | 1958a78b-86f1-4402-b9fc-9f21743a6d64 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LATIS |
| Version Model Number | 181.513 |
| Company DUNS | 139105691 |
| Company Name | GLOBUS MEDICAL, 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 | true |
| Lot Batch | true |
| Serial Number | false |
| 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(610)930-1800 |
| info@globusmedical.com |
| Length | 37 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889095048186 [Primary] |
| MAX | Intervertebral fusion device with bone graft, lumbar |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889095048186]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-02-24 |
| Device Publish Date | 2015-11-08 |
| 00889095056235 | Expanding Hex |
| 00889095056228 | Threaded Shaft, Medium |
| 00889095056211 | Threaded Shaft, Small |
| 00889095048230 | LATIS 10mm x 37mm, 8mm |
| 00889095048223 | LATIS 10mm x 37mm, 7mm |
| 00889095048216 | LATIS 10mm x 37mm, 17mm, 6° |
| 00889095048209 | LATIS 10mm x 37mm, 15mm, 6° |
| 00889095048193 | LATIS 10mm x 37mm, 14mm, 6° |
| 00889095048186 | LATIS 10mm x 37mm, 13mm, 6° |
| 00889095048179 | LATIS 10mm x 37mm, 12mm, 6° |
| 00889095048162 | LATIS 10mm x 37mm, 11mm, 6° |
| 00889095048155 | LATIS 10mm x 37mm, 10mm, 6deg; |
| 00889095048148 | LATIS 10mm x 37mm, 9mm, 6° |
| 00889095048131 | LATIS 10mm x 32mm, 8mm |
| 00889095048124 | LATIS 10mm x 32mm, 7mm |
| 00889095048117 | LATIS 10mm x 32mm, 17mm, 6° |
| 00889095048100 | LATIS 10mm x 32mm, 15mm, 6° |
| 00889095048094 | LATIS 10mm x 32mm, 14mm, 6° |
| 00889095048087 | LATIS 10mm x 32mm, 13mm, 6° |
| 00889095048070 | LATIS 10mm x 32mm, 12mm, 6° |
| 00889095048063 | LATIS 10mm x 32mm, 11mm, 6° |
| 00889095048056 | LATIS 10mm x 32mm, 10mm, 6° |
| 00889095048049 | LATIS 10mm x 32mm, 9mm, 6° |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LATIS 97581885 not registered Live/Pending |
HowGood, Inc. 2022-09-07 |
![]() LATIS 90604595 not registered Live/Pending |
Ko Yisheng 2021-03-26 |
![]() LATIS 85736592 4334782 Dead/Cancelled |
John Woodruff 2012-09-24 |
![]() LATIS 85384648 not registered Dead/Abandoned |
ACQ Company Inc. 2011-07-29 |
![]() LATIS 85366651 4419016 Live/Registered |
Globus Medical, Inc 2011-07-08 |
![]() LATIS 79103509 4204132 Dead/Cancelled |
NIPPON STEEL CORPORATION 2011-08-29 |
![]() LATIS 79103223 4204122 Dead/Cancelled |
NIPPON STEEL CORPORATION 2011-08-29 |
![]() LATIS 77212185 not registered Dead/Abandoned |
Globus Medical, Inc. 2007-06-21 |
![]() LATIS 76502786 2971800 Dead/Cancelled |
Integrated Health Essentials, Inc. 2003-03-27 |
![]() LATIS 76157014 not registered Dead/Abandoned |
Latis Networks, Inc 2000-10-30 |
![]() LATIS 76156881 not registered Dead/Abandoned |
Latis Networks, Inc. 2000-10-30 |
![]() LATIS 76141737 not registered Dead/Abandoned |
Latis Networks, Inc. 2000-10-03 |