Artix MT 32-101

GUDID 00850291007345

Thrombectomy wire-net

Primary Device ID	00850291007345
NIH Device Record Key	d43dd6c6-03fa-4131-97e2-620c2dcfd5f0
Commercial Distribution Status	In Commercial Distribution
Brand Name	Artix MT
Version Model Number	32-101
Catalog Number	32-101
Company DUNS	076827459
Company Name	INARI MEDICAL INC
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00850291007345 [Primary]

QEW	Peripheral Mechanical Thrombectomy With Aspiration

Steralize Prior To Use	false
Device Is Sterile	true

00850291007345	Artix™ MT
00810123710591	Artix MT (Thrombectomy Device)
00810123710584	Artix MT (Thrombectomy Device)