gudid
Primary ID: 32-103 / AS-01244
Artix MT (UDI 32-103 / AS-01244)
Manufactured by Inari Medical, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Artix MT - Primary ID 32-103 / AS-01244
Device Regulatory Overview
The Artix MT (Model/Catalog Number: 32-103 / AS-01244) is a medical device manufactured by Inari Medical, Inc.. This product is indexed under FDA Product Code / Category Classification QEW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 32-103 / AS-01244
- Product Code / EMDN
- QEW
- Device Name
- Artix MT (Thrombectomy Device)
- Database Sync Date
- 2026-08-09 09:12:26
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Artix MT?
The registered manufacturer of record for Artix MT is Inari Medical, Inc..
What is the Primary UDI-DI identifier for Artix MT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 32-103 / AS-01244.
What classification code is assigned to this device?
This device is registered under product classification code QEW.
Similar Classification Devices (QEW)
Other Devices by Inari Medical, Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint