| Primary Device ID | 00813153024898 |
| NIH Device Record Key | 85a5dcdd-52a9-482c-a6c7-362031e36ce2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Codan |
| Version Model Number | BC 2085 |
| 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 | 00813153024898 [Package] Contains: 10813153024895 Package: [1 Units] In Commercial Distribution |
| GS1 | 10813153024895 [Primary] |
| FPA | Set, Administration, Intravascular |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2024-10-03 |
| Device Publish Date | 2018-05-31 |
| 00813153024898 | Extension Set with Needlefree Valves |
| 00813153027486 | NICU MEDICATION ADMINISTRATION SET |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CODAN 79230793 5876184 Live/Registered |
CODAN Holding GmbH 2017-06-14 |
![]() CODAN 79182078 5197701 Live/Registered |
Codan Holding GmbH 2015-12-02 |
![]() CODAN 79173738 4990899 Live/Registered |
CODAN, S.A. 2015-07-20 |
![]() CODAN 79126780 4503627 Live/Registered |
Codan Rubber Danmark A/S 2013-01-29 |
![]() CODAN 77832492 3917799 Live/Registered |
Codan Limited 2009-09-22 |
![]() CODAN 73636665 1638977 Live/Registered |
CODAN MEDIZINISCHE GERATE GMBH & CO KOMMANDITGESELLSCHAFT 1986-12-22 |