Primary Device ID | 10821684009021 |
NIH Device Record Key | be8cea92-ff26-4ac0-a40e-db4f08868ed9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NITREX |
Version Model Number | N143001 |
Company DUNS | 968903703 |
Company Name | Covidien LP |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
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 |
Outer Diameter | 0.014 Inch |
Length | 300 Centimeter |
Device Size Text, specify | 0 |
Outer Diameter | 0.014 Inch |
Length | 300 Centimeter |
Device Size Text, specify | 0 |
Outer Diameter | 0.014 Inch |
Length | 300 Centimeter |
Device Size Text, specify | 0 |
Outer Diameter | 0.014 Inch |
Length | 300 Centimeter |
Device Size Text, specify | 0 |
Outer Diameter | 0.014 Inch |
Length | 300 Centimeter |
Device Size Text, specify | 0 |
Outer Diameter | 0.014 Inch |
Length | 300 Centimeter |
Device Size Text, specify | 0 |
Outer Diameter | 0.014 Inch |
Length | 300 Centimeter |
Device Size Text, specify | 0 |
Outer Diameter | 0.014 Inch |
Length | 300 Centimeter |
Device Size Text, specify | 0 |
Outer Diameter | 0.014 Inch |
Length | 300 Centimeter |
Device Size Text, specify | 0 |
Outer Diameter | 0.014 Inch |
Length | 300 Centimeter |
Device Size Text, specify | 0 |
Outer Diameter | 0.014 Inch |
Length | 300 Centimeter |
Device Size Text, specify | 0 |
Outer Diameter | 0.014 Inch |
Length | 300 Centimeter |
Device Size Text, specify | 0 |
Outer Diameter | 0.014 Inch |
Length | 300 Centimeter |
Device Size Text, specify | 0 |
Outer Diameter | 0.014 Inch |
Length | 300 Centimeter |
Device Size Text, specify | 0 |
Outer Diameter | 0.014 Inch |
Length | 300 Centimeter |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10821684009021 [Primary] |
DQX | WIRE, GUIDE, CATHETER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2024-05-20 |
Device Publish Date | 2015-10-12 |
10821684001414 | Guidewire |
10821684009281 | Guidewire |
10821684009274 | Guidewire |
10821684009267 | Guidewire |
10821684009250 | Guidewire |
10821684009243 | Guidewire |
10821684009236 | Guidewire |
10821684009229 | Guidewire |
10821684009212 | Guidewire |
10821684009205 | Guidewire |
10821684009199 | Guidewire |
10821684009182 | Guidewire |
10821684009175 | Guidewire |
10821684009151 | Guidewire |
10821684009144 | Guidewire |
10821684009137 | Guidewire |
10821684009120 | Guidewire |
10821684009113 | Guidewire |
10821684009106 | Guidewire |
10821684009090 | Guidewire |
10821684009083 | Guidewire |
10821684009076 | Guidewire |
10821684009069 | Guidewire |
10821684009052 | Guidewire |
10821684009045 | Guidewire |
10821684009038 | Guidewire |
10821684009021 | Guidewire |
10821684009014 | Guidewire |
10821684009007 | Guidewire |
10821684001438 | Guidewire |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NITREX 86226045 not registered Dead/Abandoned |
Delta Medical Systems, Inc. 2014-03-19 |
NITREX 86226045 not registered Dead/Abandoned |
Delta Medical Supply Group, Inc. 2014-03-19 |
NITREX 78211793 2957976 Live/Registered |
COVIDIEN LP 2003-02-06 |
NITREX 77857510 3847324 Live/Registered |
Eva-Glory Industrial Co., Ltd 2009-10-26 |
NITREX 77590522 3962222 Dead/Cancelled |
Alliant Techsystems Inc. 2008-10-10 |
NITREX 77482734 3590376 Dead/Cancelled |
American Agritech, LLC 2008-05-23 |
NITREX 77141162 3664109 Dead/Cancelled |
Alliant Techsystems Inc. 2007-03-27 |
NITREX 77141005 not registered Dead/Abandoned |
Alliant Techsystems Inc. 2007-03-27 |
NITREX 77140999 not registered Dead/Abandoned |
Alliant Techsystems Inc. 2007-03-27 |
NITREX 76508904 2824773 Live/Registered |
DELTA MEDICAL SYSTEMS, INC. 2003-04-23 |
NITREX 76508904 2824773 Live/Registered |
DELTA HOSPITAL SUPPLY, INC. 2003-04-23 |
NITREX 76508904 2824773 Live/Registered |
DELTA MEDICAL SUPPLY GROUP, INC. 2003-04-23 |