NITREX

GUDID 10821684009182

Guidewire

Covidien LP

Cardiac/peripheral vascular guidewire, single-use
Primary Device ID10821684009182
NIH Device Record Keye6c74aa8-555e-43b7-93cd-872846656c59
Commercial Distribution StatusIn Commercial Distribution
Brand NameNITREX
Version Model NumberN351805
Company DUNS968903703
Company NameCovidien LP
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com

Device Dimensions

Length180 Centimeter
Outer Diameter0.035 Inch
Device Size Text, specify0
Length180 Centimeter
Outer Diameter0.035 Inch
Device Size Text, specify0
Length180 Centimeter
Outer Diameter0.035 Inch
Device Size Text, specify0
Length180 Centimeter
Outer Diameter0.035 Inch
Device Size Text, specify0
Length180 Centimeter
Outer Diameter0.035 Inch
Device Size Text, specify0
Length180 Centimeter
Outer Diameter0.035 Inch
Device Size Text, specify0
Length180 Centimeter
Outer Diameter0.035 Inch
Device Size Text, specify0
Length180 Centimeter
Outer Diameter0.035 Inch
Device Size Text, specify0
Length180 Centimeter
Outer Diameter0.035 Inch
Device Size Text, specify0
Length180 Centimeter
Outer Diameter0.035 Inch
Device Size Text, specify0
Length180 Centimeter
Outer Diameter0.035 Inch
Device Size Text, specify0

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry

Device Identifiers

Device Issuing AgencyDevice ID
GS110821684009182 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DQXWIRE, GUIDE, CATHETER

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2024-05-02
Device Publish Date2015-10-12

On-Brand Devices [NITREX]

10821684001414Guidewire
10821684009281Guidewire
10821684009274Guidewire
10821684009267Guidewire
10821684009250Guidewire
10821684009243Guidewire
10821684009236Guidewire
10821684009229Guidewire
10821684009212Guidewire
10821684009205Guidewire
10821684009199Guidewire
10821684009182Guidewire
10821684009175Guidewire
10821684009151Guidewire
10821684009144Guidewire
10821684009137Guidewire
10821684009120Guidewire
10821684009113Guidewire
10821684009106Guidewire
10821684009090Guidewire
10821684009083Guidewire
10821684009076Guidewire
10821684009069Guidewire
10821684009052Guidewire
10821684009045Guidewire
10821684009038Guidewire
10821684009021Guidewire
10821684009014Guidewire
10821684009007Guidewire
10821684001438Guidewire

Trademark Results [NITREX]

Mark Image

Registration | Serial
Company
Trademark
Application Date
NITREX
NITREX
86226045 not registered Dead/Abandoned
Delta Medical Systems, Inc.
2014-03-19
NITREX
NITREX
86226045 not registered Dead/Abandoned
Delta Medical Supply Group, Inc.
2014-03-19
NITREX
NITREX
78211793 2957976 Live/Registered
COVIDIEN LP
2003-02-06
NITREX
NITREX
77857510 3847324 Live/Registered
Eva-Glory Industrial Co., Ltd
2009-10-26
NITREX
NITREX
77590522 3962222 Dead/Cancelled
Alliant Techsystems Inc.
2008-10-10
NITREX
NITREX
77482734 3590376 Dead/Cancelled
American Agritech, LLC
2008-05-23
NITREX
NITREX
77141162 3664109 Dead/Cancelled
Alliant Techsystems Inc.
2007-03-27
NITREX
NITREX
77141005 not registered Dead/Abandoned
Alliant Techsystems Inc.
2007-03-27
NITREX
NITREX
77140999 not registered Dead/Abandoned
Alliant Techsystems Inc.
2007-03-27
NITREX
NITREX
76508904 2824773 Live/Registered
DELTA MEDICAL SYSTEMS, INC.
2003-04-23
NITREX
NITREX
76508904 2824773 Live/Registered
DELTA HOSPITAL SUPPLY, INC.
2003-04-23
NITREX
NITREX
76508904 2824773 Live/Registered
DELTA MEDICAL SUPPLY GROUP, INC.
2003-04-23

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