FDA UDI In Commercial Distribution 🇺🇸 United States

Artix BG

DI: 00850291007321 · Model: 30-101 · INARI MEDICAL INC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Artix BG
Primary DI
00850291007321
Version / Model
30-101
Catalog Number
30-101
Company Name
INARI MEDICAL INC
Labeler DUNS
076827459
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-09
Public Version
2
Public Version Date
2023-12-04
Public Version Status
Update
Public Device Record Key
c389e944-0128-4b61-8146-9c0d5080ab3d

Device Description

Artix BG (65cm)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
QEW Peripheral Mechanical Thrombectomy With Aspiration
DQY Catheter, Percutaneous

GMDN Terms

Code Name
32584 Intravascular occluding balloon catheter, image-guided

Identifiers

Type ID
Primary 00850291007321

Customer Contacts

Phone
877-923-4747

Premarket Submissions

Submission Number Supplement Number
K221846 000
K223000 000
K230912 000