NITREX™

GUDID 00821684058381

GW N353001 NITREX V03

Covidien LP

Peripheral vascular guidewire, manual
Primary Device ID00821684058381
NIH Device Record Key666a7ca6-d7d7-41d7-a1c8-04457da9f1e5
Commercial Distribution StatusIn Commercial Distribution
Brand NameNITREX™
Version Model NumberN353001
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.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
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Length300 Centimeter
Outer Diameter0.89 Millimeter
Device Size Text, specify0
Length300 Centimeter
Outer Diameter0.89 Millimeter
Device Size Text, specify0
Length300 Centimeter
Outer Diameter0.89 Millimeter
Device Size Text, specify0
Length300 Centimeter
Outer Diameter0.89 Millimeter
Device Size Text, specify0
Length300 Centimeter
Outer Diameter0.89 Millimeter
Device Size Text, specify0
Length300 Centimeter
Outer Diameter0.89 Millimeter
Device Size Text, specify0
Length300 Centimeter
Outer Diameter0.89 Millimeter
Device Size Text, specify0
Length300 Centimeter
Outer Diameter0.89 Millimeter
Device Size Text, specify0
Length300 Centimeter
Outer Diameter0.89 Millimeter
Device Size Text, specify0
Length300 Centimeter
Outer Diameter0.89 Millimeter
Device Size Text, specify0
Length300 Centimeter
Outer Diameter0.89 Millimeter
Device Size Text, specify0
Length300 Centimeter
Outer Diameter0.89 Millimeter
Device Size Text, specify0
Length300 Centimeter
Outer Diameter0.89 Millimeter
Device Size Text, specify0
Length300 Centimeter
Outer Diameter0.89 Millimeter
Device Size Text, specify0
Length300 Centimeter
Device Size Text, specify0
Outer Diameter0.035 Inch
Length300 Centimeter
Device Size Text, specify0
Outer Diameter0.035 Inch
Length300 Centimeter
Device Size Text, specify0
Outer Diameter0.035 Inch
Length300 Centimeter
Device Size Text, specify0
Outer Diameter0.035 Inch
Length300 Centimeter
Device Size Text, specify0
Outer Diameter0.035 Inch
Length300 Centimeter
Device Size Text, specify0
Outer Diameter0.035 Inch
Length300 Centimeter
Device Size Text, specify0
Outer Diameter0.035 Inch
Length300 Centimeter
Device Size Text, specify0
Outer Diameter0.035 Inch
Length300 Centimeter
Device Size Text, specify0
Outer Diameter0.035 Inch
Length300 Centimeter
Device Size Text, specify0
Outer Diameter0.035 Inch
Length300 Centimeter
Device Size Text, specify0
Outer Diameter0.035 Inch

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Do not store in direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Do not store in direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Do not store in direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Do not store in direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Do not store in direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Do not store in direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Do not store in direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Do not store in direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Do not store in direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Do not store in direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Do not store in direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Do not store in direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Do not store in direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Do not store in direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Do not store in direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Do not store in direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Do not store in direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Do not store in direct sunlight
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
GS100821684058381 [Primary]
GS100821684065532 [Package]
Package: PK [3 Units]
In Commercial Distribution

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 Number3
Public Version Date2018-07-06
Device Publish Date2017-06-16

On-Brand Devices [NITREX™]

00821684058404GW N354002 NITREX V03
00821684058398GW N354001 NITREX V03
00821684058381GW N353001 NITREX V03
00821684058374GW N352604 NITREX V03
00821684058367GW N352603 NITREX V03
00821684058350GW N352602 NITREX V03
00821684058343GW N352601 NITREX V03
00821684058336GW N351805 NITREX V03
00821684058329GW N351804 NITREX V03
00821684058312GW N351803 NITREX V03
00821684058305GW N351455 NITREX V03
00821684058299GW N351454 NITREX V03
00821684058282GW N351453 NITREX V03
00821684058275GW N351452 NITREX V03
00821684058268GW N351451 NITREX V03
00821684058251GW N350801 NITREX V03
00821684058244GW N252601 NITREX V03
00821684058237GW N251802 NITREX V03
00821684058220GW N251801 NITREX V03
00821684058213GW N183002 NITREX V03
00821684058206GW N183001 NITREX V03
00821684058190GW N181806 NITREX V03
00821684058183GW N181805 NITREX V03
00821684058176GW N181804 NITREX V03
00821684058169GW N180802 NITREX V03
00821684058152GW N180801 NITREX V03
00821684058145GW N180603 NITREX V03
00821684058138GW N180601 NITREX V03
00821684058121GW N143001 NITREX V03
00821684058114GW N141802 NITREX V03
00821684058107GW N140801 NITREX V03

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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