HI-TORQUE EXTRA S'PORT 22225M-175

GUDID 28717648079584

HI-TORQUE EXTRA S'PORT Guide Wire .014 Straight Tip 3.0 cm x 175 cm

ABBOTT VASCULAR INC.

Cardiac/peripheral vascular guidewire, single-use
Primary Device ID28717648079584
NIH Device Record Keya4a089c7-2409-454a-a5d3-7f738d040742
Commercial Distribution StatusIn Commercial Distribution
Brand NameHI-TORQUE EXTRA S'PORT
Version Model Number22225M-175
Catalog Number22225M-175
Company DUNS964569052
Company NameABBOTT VASCULAR INC.
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(800)227-9902
EmailAV.CUSTOMERCARE@AV.ABBOTT.COM
Phone+1(800)227-9902
EmailAV.CUSTOMERCARE@AV.ABBOTT.COM
Phone+1(800)227-9902
EmailAV.CUSTOMERCARE@AV.ABBOTT.COM
Phone+1(800)227-9902
EmailAV.CUSTOMERCARE@AV.ABBOTT.COM
Phone+1(800)227-9902
EmailAV.CUSTOMERCARE@AV.ABBOTT.COM
Phone+1(800)227-9902
EmailAV.CUSTOMERCARE@AV.ABBOTT.COM
Phone+1(800)227-9902
EmailAV.CUSTOMERCARE@AV.ABBOTT.COM
Phone+1(800)227-9902
EmailAV.CUSTOMERCARE@AV.ABBOTT.COM
Phone+1(800)227-9902
EmailAV.CUSTOMERCARE@AV.ABBOTT.COM
Phone+1(800)227-9902
EmailAV.CUSTOMERCARE@AV.ABBOTT.COM
Phone+1(800)227-9902
EmailAV.CUSTOMERCARE@AV.ABBOTT.COM
Phone+1(800)227-9902
EmailAV.CUSTOMERCARE@AV.ABBOTT.COM
Phone+1(800)227-9902
EmailAV.CUSTOMERCARE@AV.ABBOTT.COM
Phone+1(800)227-9902
EmailAV.CUSTOMERCARE@AV.ABBOTT.COM
Phone+1(800)227-9902
EmailAV.CUSTOMERCARE@AV.ABBOTT.COM
Phone+1(800)227-9902
EmailAV.CUSTOMERCARE@AV.ABBOTT.COM
Phone+1(800)227-9902
EmailAV.CUSTOMERCARE@AV.ABBOTT.COM
Phone+1(800)227-9902
EmailAV.CUSTOMERCARE@AV.ABBOTT.COM

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Stored in a dry, dark, cool place
Special Storage Condition, SpecifyBetween 0 and 0 *Stored in a dry, dark, cool place
Special Storage Condition, SpecifyBetween 0 and 0 *Stored in a dry, dark, cool place
Special Storage Condition, SpecifyBetween 0 and 0 *Stored in a dry, dark, cool place
Special Storage Condition, SpecifyBetween 0 and 0 *Stored in a dry, dark, cool place
Special Storage Condition, SpecifyBetween 0 and 0 *Stored in a dry, dark, cool place
Special Storage Condition, SpecifyBetween 0 and 0 *Stored in a dry, dark, cool place
Special Storage Condition, SpecifyBetween 0 and 0 *Stored in a dry, dark, cool place
Special Storage Condition, SpecifyBetween 0 and 0 *Stored in a dry, dark, cool place
Special Storage Condition, SpecifyBetween 0 and 0 *Stored in a dry, dark, cool place
Special Storage Condition, SpecifyBetween 0 and 0 *Stored in a dry, dark, cool place
Special Storage Condition, SpecifyBetween 0 and 0 *Stored in a dry, dark, cool place
Special Storage Condition, SpecifyBetween 0 and 0 *Stored in a dry, dark, cool place
Special Storage Condition, SpecifyBetween 0 and 0 *Stored in a dry, dark, cool place
Special Storage Condition, SpecifyBetween 0 and 0 *Stored in a dry, dark, cool place
Special Storage Condition, SpecifyBetween 0 and 0 *Stored in a dry, dark, cool place
Special Storage Condition, SpecifyBetween 0 and 0 *Stored in a dry, dark, cool place
Special Storage Condition, SpecifyBetween 0 and 0 *Stored in a dry, dark, cool place

Device Identifiers

Device Issuing AgencyDevice ID
GS108717648079580 [Primary]
GS128717648079584 [Package]
Contains: 08717648079580
Package: Case [5 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 Number5
Public Version Date2020-03-23
Device Publish Date2016-02-19