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 |