TORQUE DEVICE 1003279

GUDID 28717648013922

.035 Torque Device

ABBOTT VASCULAR INC.

Torque manipulation device
Primary Device ID28717648013922
NIH Device Record Key20e819bd-2dc5-4730-810f-a01daf5b9b34
Commercial Distribution StatusIn Commercial Distribution
Brand NameTORQUE DEVICE
Version Model Number1003279
Catalog Number1003279
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

Operating and Storage Conditions

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

Device Identifiers

Device Issuing AgencyDevice ID
GS108717648013928 [Primary]
GS128717648013922 [Package]
Contains: 08717648013928
Package: Case [10 Units]
In Commercial Distribution

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 Number4
Public Version Date2020-03-23
Device Publish Date2016-08-05

On-Brand Devices [TORQUE DEVICE]

28717648013922.035 Torque Device
28717648013298Torque Device

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