Primary Device ID | 00855318006240 |
NIH Device Record Key | b5b2a028-1b95-41e0-833d-40ed3638ef38 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Maxxeus |
Version Model Number | XK010 |
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 | 00855318006240 [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 |