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 |