FlowStasis Single-Pack 70-103

GUDID 00850291007420

FlowStasis Single-Pack

INARI MEDICAL INC

Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device

• Primary Device ID: 00850291007420
• NIH Device Record Key: 967d0aeb-9628-40b3-9e17-4cf756498f70
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FlowStasis Single-Pack
• Version Model Number: 70-103
• Catalog Number: 70-103
• Company DUNS: 076827459
• Company Name: INARI MEDICAL INC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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
• Phone: 18779234747
• Email: info@inarimedical.com
• Phone: 18779234747
• Email: info@inarimedical.com
• Phone: 18779234747
• Email: info@inarimedical.com
• Phone: 18779234747
• Email: info@inarimedical.com
• Phone: 18779234747
• Email: info@inarimedical.com
• Phone: 18779234747
• Email: info@inarimedical.com
• Phone: 18779234747
• Email: info@inarimedical.com
• Phone: 18779234747
• Email: info@inarimedical.com
• Phone: 18779234747
• Email: info@inarimedical.com
• 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	00850291007420 [Primary]

FDA Product Code

• KGS: Retention Device, Suture

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: 2023-07-27
• Device Publish Date: 2023-07-19

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• 00810123710522 - Triever20 Curve: 2023-12-25 Triever20 Curve