| Primary Device ID | 00813153026557 |
| NIH Device Record Key | 5000e8e3-1fbf-4f73-a14e-dafab0362ddd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Rem Systems |
| Version Model Number | BC 2151 |
| Company DUNS | 058027475 |
| Company Name | CODAN US CORPORATION |
| 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 | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00813153026557 [Package] Contains: 10813153026554 Package: [1 Units] In Commercial Distribution |
| GS1 | 10813153026554 [Primary] |
| FPA | Set, Administration, Intravascular |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-04-08 |
| Device Publish Date | 2021-03-31 |
| 00813153025406 | 200 Micron Filter Unit for Stem Cell Infusions |
| 00813153026557 | Extension Set with Ultra-Clear Valve |
| 00897891001588 | Blood Set with Stopcock, Check Valve & Needlefree Valve |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() REM SYSTEMS 78495791 3152853 Dead/Cancelled |
REM SYSTEMS, INC. 2004-10-06 |
![]() REM SYSTEMS 74124460 not registered Dead/Abandoned |
Rem Systems, Inc. 1990-12-13 |