Mobi-C MB3796
GUDID 03662663002059
MOBI-C IMPLANT M « STANDARD » 17x19 H6 US
LDR Spine Usa, Inc.
Cervical total disc replacement prosthesis Cervical total intervertebral disc replacement prosthesis Cervical total intervertebral disc replacement prosthesis Cervical total intervertebral disc replacement prosthesis Cervical total intervertebral disc replacement prosthesis Cervical total intervertebral disc replacement prosthesis Cervical total intervertebral disc replacement prosthesis Cervical total intervertebral disc replacement prosthesis Cervical total intervertebral disc replacement prosthesis Cervical total intervertebral disc replacement prosthesis Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular Cervical total intervertebral disc prosthesis, modular| Primary Device ID | 03662663002059 |
| NIH Device Record Key | 55d2907f-1c56-4dd4-8f04-b38e51e77855 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mobi-C |
| Version Model Number | MB3796 |
| Catalog Number | MB3796 |
| Company DUNS | 615789729 |
| Company Name | LDR Spine Usa, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com |
Device Dimensions
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
| Width | 19 Millimeter |
| Depth | 17 Millimeter |
| Height | 6 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03662663002059 [Primary] |
FDA Product Code
| MJO | Prosthesis, Intervertebral Disc |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-04-06 |
| Device Publish Date | 2017-04-12 |
On-Brand Devices [Mobi-C]
| 03662663002097 | MOBI-C IMPLANT M « STANDARD » 19x19 H7 US |
| 03662663002080 | MOBI-C IMPLANT M « STANDARD » 19x19 H6 US |
| 03662663002073 | MOBI-C IMPLANT M « STANDARD » 19x19 H5 US |
| 03662663002066 | MOBI-C IMPLANT M « STANDARD » 17x19 H7 US |
| 03662663002059 | MOBI-C IMPLANT M « STANDARD » 17x19 H6 US |
| 03662663002042 | MOBI-C IMPLANT M « STANDARD » 17x19 H5 US |
| 03662663002035 | MOBI-C IMPLANT M « STANDARD » 17x17 H7 US |
| 03662663002028 | MOBI-C IMPLANT M « STANDARD » 17x17 H6 US |
| 03662663002011 | MOBI-C IMPLANT M « STANDARD » 17x17 H5 US |
| 03662663000253 | MB917R |
| 03662663000437 | MB949R |
| 03662663000420 | MB948R |
| 03662663000413 | MB947R |
| 03662663000406 | MB946R |
| 03662663000390 | MB945R |
| 03662663000383 | MB944R |
| 03662663000376 | MB943R |
| 03662663000369 | MB942R |
| 03662663000246 | MB906R |
| 03662663000239 | MB904R |
| 03662663000222 | MB903R |
| 03662663000215 | MB900R |
Trademark Results [Mobi-C]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MOBI-C 78514826 3197424 Live/Registered |
LDR MEDICAL, S.A.S. 2004-11-10 |
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