FlowTriever

GUDID 00850291007062

FlowTriever Catheter, 18 mm, SS

INARI MEDICAL INC

Thrombectomy suction catheter

• Primary Device ID: 00850291007062
• NIH Device Record Key: 5173f36e-fca6-474a-9ccb-deeb2484f0ce
• Commercial Distribution Discontinuation: 2016-12-07
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: FlowTriever
• Version Model Number: 10-105
• 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: 19496008433
• Email: info@inarimedical.com
• Phone: 19496008433
• Email: info@inarimedical.com
• Phone: 19496008433
• Email: info@inarimedical.com
• Phone: 19496008433
• Email: info@inarimedical.com
• Phone: 19496008433
• Email: info@inarimedical.com
• Phone: 19496008433
• Email: info@inarimedical.com
• Phone: 19496008433
• Email: info@inarimedical.com
• Phone: 19496008433
• Email: info@inarimedical.com
• Phone: 19496008433
• Email: info@inarimedical.com
• Phone: 19496008433
• Email: info@inarimedical.com
• Phone: 19496008433
• Email: info@inarimedical.com
• Phone: 19496008433
• Email: info@inarimedical.com

Device Dimensions

• Outer Diameter: 18 Millimeter
• Outer Diameter: 18 Millimeter
• Outer Diameter: 18 Millimeter
• Outer Diameter: 18 Millimeter
• Outer Diameter: 18 Millimeter
• Outer Diameter: 18 Millimeter
• Outer Diameter: 18 Millimeter
• Outer Diameter: 18 Millimeter
• Outer Diameter: 18 Millimeter
• Outer Diameter: 18 Millimeter
• Outer Diameter: 18 Millimeter
• Outer Diameter: 18 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850291007062 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K143563

FDA Product Code

• DXE: Catheter, Embolectomy

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-04
• Device Publish Date: 2016-09-15

On-Brand Devices [FlowTriever]

• 00850291007086: Retraction Aspirator, Single Insertion
• 00850291007062: FlowTriever Catheter, 18 mm, SS
• 00850291007048: Retraction Aspirator
• 00850291007031: Aspiration Guide Catheter