| Primary Device ID | 00852371006095 |
| NIH Device Record Key | 10b6a8cf-39d1-4517-bb09-4274198ff52b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | OsteoMatrix |
| Version Model Number | OMCS05 |
| Catalog Number | OMCS05 |
| Company DUNS | 827042487 |
| Company Name | BIOSTRUCTURES, LLC |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Length | 15 Millimeter |
| Length | 15 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00852371006095 [Primary] |
| MQV | Filler, Bone Void, Calcium Compound |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[00852371006095]
Radiation Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2015-11-09 |
| 00852371006095 | Mineralized Collagen Scaffold |
| 00852371006088 | Mineralized Collagen Scaffold |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() OSTEOMATRIX 77248497 3696376 Live/Registered |
BIOVENTUS LLC 2007-08-06 |
![]() OSTEOMATRIX 76283675 not registered Dead/Abandoned |
Osteomedical Ltd. UK 2001-07-12 |
![]() OSTEOMATRIX 76009243 3121063 Live/Registered |
SHAKLEE CORPORATION 2000-03-24 |
![]() OSTEOMATRIX 75311519 not registered Dead/Abandoned |
Osteomedical Ltd. 1997-06-19 |