| Primary Device ID | 00855318006257 |
| NIH Device Record Key | e6ebf1c2-953a-43b3-8990-8f7e95775637 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Maxxeus |
| Version Model Number | XK020 |
| Company DUNS | 071276372 |
| Company Name | FOUNDATION FOR COMMUNITY BLOOD CENTER/COMMUNITY TISSUE SERVICES, THE |
| 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 | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00855318006257 [Primary] |
| NPM | Bone Grafting Material, Animal Source |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-08-30 |
| Device Publish Date | 2018-07-30 |
| 00855318006325 | OL005 |
| 00855318006318 | OK005 |
| 00855318006301 | OK025 |
| 00855318006295 | XL080 |
| 00855318006288 | XL040 |
| 00855318006271 | XL020 |
| 00855318006264 | XK040 |
| 00855318006257 | XK020 |
| 00855318006240 | XK010 |
| 00855318006233 | XK005 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MAXXEUS 86708549 5071123 Live/Registered |
Community Blood Center 2015-07-29 |
![]() MAXXEUS 86347304 not registered Dead/Abandoned |
Community Blood Center 2014-07-24 |
![]() MAXXEUS 85246270 4184015 Live/Registered |
Community Blood Center 2011-02-18 |