Artix Thin-Walled Sheath

GUDID 00810123710577

Artix Thin-Walled Sheath

INARI MEDICAL INC

Thrombectomy wire-net

• Primary Device ID: 00810123710577
• NIH Device Record Key: 20f4d20d-bd37-41e6-8fe5-1186c8fae68d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Artix Thin-Walled Sheath
• Version Model Number: 30-104 / AS-01206
• 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

Customer Support Contacts

• Phone: 18779234747
• Email: info@inarimedical.com
• Phone: 18779234747
• Email: info@inarimedical.com
• Phone: 18779234747
• Email: info@inarimedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810123710577 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K241894

FDA Product Code

• KRA: Catheter, Continuous Flush

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-19
• Device Publish Date: 2024-11-11

On-Brand Devices [Artix Thin-Walled Sheath]

• 00810123710560: Artix Thin-Walled Sheath (Thrombectomy Sheath)
• 00810123710577: Artix Thin-Walled Sheath