Primary Device ID | 10884521174009 |
NIH Device Record Key | 32ac7541-8e7b-4dfe-846f-d5ae081df7f6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Covidien |
Version Model Number | 8881389459 |
Catalog Number | 8881389459 |
Company DUNS | 080935429 |
Company Name | Cardinal Health, Inc. |
Device Count | 400 |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10884521174009 [Primary] |
GS1 | 20884521174006 [Unit of Use] |
GIM | Tubes, vacuum sample, with anticoagulant |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2021-03-19 |
Device Publish Date | 2016-09-24 |
50885380169494 | True content to be populated as part of rebranding |
50885380167162 | Grifols 3038172 TRNSF NDL 20X1.625B |
50885380167155 | Grifols 3037908 FLTR NDL 16X.75I |
10885380170096 | True content to be populated as part of rebranding |
10885380169779 | Kendall DL Disposable Lead Set |
10884521158795 | True content to be populated as part of rebranding |
10884521162624 | HDNDL-E 27X 7/8RBT SMK GRA 11M |
20884521661629 | True content to be populated as part of rebranding |
10192253002058 | Cardinal Health Quilted Premium Strength XXL Underpads Wings |
10884521768109 | True content to be populated as part of rebranding |
10884521643185 | NuPrep Gel |
10884521643178 | Neurodiagnostic Electrode Paste |
20884521643168 | Neurodiagnostic Electrode Paste |
10884521746886 | DL System Direct Connect Philips MX40 Masimo SPO2 5 Lead |
10884521746862 | DL System Direct Connect Philips MX40 Nellcor SPO2 5 Lead |
10884521517325 | KDL System Radiolucent 5 Lead 36" V-lead |
10884521517257 | Kendall DL Disposable Lead Set 5 Lead Radiolucent |
10884521517233 | Kendall DL Disposable Lead Set |
10884521180390 | True content to be populated as part of rebranding |
10884521174009 | True content to be populated as part of rebranding |
10884521717404 | DL System Direct Connect Philips MX40 Non SPO2 5 Lead |
10884521517349 | True content to be populated as part of rebranding |
10884521517332 | TBD during rebranding |
10884521517264 | True content to be populated as part of rebranding |
10884521517158 | True content to be populated as part of rebranding |
10884521517141 | True content to be populated as part of rebranding |
10884521517134 | TBD during rebranding |
10884521517127 | TBD during rebranding |
20884521189222 | True content to be populated as part of rebranding |
20884521722276 | Naso-Jejunal Feeding Tube with ENFit Connection |
30884521742592 | Safety Needle, Thin Wall, 20 Gauge x 1.5 Inch, Bulk, Non-sterile |
20884521661759 | True content to be populated as part of rebranding |
20884521661742 | True content to be populated as part of rebranding |
20884521661735 | True content to be populated as part of rebranding |
20884521661728 | Gastro Feeding Tube with ENfit Y-Port 22FR |
20884521661711 | True content to be populated as part of rebranding |
20884521661704 | True content to be populated as part of rebranding |
10884521661691 | Gastronomy Feed Tube With ENFit Y-Port 16FR |
20884521661636 | Gastro Feed Tube With ENFit Y-Port 14FR |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
COVIDIEN 90304387 not registered Live/Pending |
Covidien AG 2020-11-06 |
COVIDIEN 85304633 4156643 Dead/Cancelled |
Covidien AG 2011-04-26 |
COVIDIEN 85200339 3997421 Live/Registered |
Covidien AG 2010-12-17 |
COVIDIEN 77658013 3951342 Dead/Cancelled |
Covidien AG 2009-01-28 |
COVIDIEN 77653157 3679078 Dead/Cancelled |
Covidien AG 2009-01-21 |
COVIDIEN 77160146 3524947 Dead/Cancelled |
Covidien AG 2007-04-18 |
COVIDIEN 77160140 3361986 Dead/Cancelled |
Covidien AG 2007-04-18 |
COVIDIEN 77160115 3582123 Live/Registered |
Covidien AG 2007-04-18 |