Artix AX

GUDID 00810123710256

Artix AX, 115cm

INARI MEDICAL INC

Thrombectomy suction catheter
Primary Device ID00810123710256
NIH Device Record Key40f782e6-c014-4e80-98c3-226ca55a9002
Commercial Distribution StatusIn Commercial Distribution
Brand NameArtix AX
Version Model Number31-102
Company DUNS076827459
Company NameINARI MEDICAL 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

Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100810123710256 [Primary]
GS100850291007376 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

QEWPeripheral Mechanical Thrombectomy With Aspiration

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-01-14
Device Publish Date2026-01-06

On-Brand Devices [Artix AX]

00810123710256Artix AX, 115cm
00810123710249Artix AX, 85cm

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