| Primary Device ID | 00812337021043 |
| NIH Device Record Key | dd01af3a-c0f4-4d39-a90f-ebfc1547a3e1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CopiOs® Bone Void Filler Sponge |
| Version Model Number | 20101-01 |
| Catalog Number | 00-1103-010-01 |
| Company DUNS | 131107757 |
| Company Name | DSM BIOMEDICAL, 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Total Volume | 1 Milliliter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00812337021043 [Primary] |
| MQV | Filler, Bone Void, Calcium Compound |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-02-13 |
| Device Publish Date | 2015-09-17 |
| 00812337021067 | 20101-03 |
| 00812337021050 | 20101-02 |
| 00812337021043 | 20101-01 |
| 00812337021036 | 20100-03 |
| 00812337021029 | Sponge |
| 00812337021012 | 20100-01 |
| M2630700582004 | 20100-03 |
| M2630700582003 | 20100-02 |
| M2630700582001 | 20100-01 |
| M2630011301001 | 20101-01 |
| M26300110301010 | 20101-03 |
| M26300110301005 | 20101-02 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() COPIOS 76520337 3130249 Live/Registered |
ZIMMER, INC. 2003-05-20 |