LimFlow Crossing Stent Graft

GUDID 00850041730165

LimFlow Crossing Stent Graft (3.5-5.5 mm x 60 mm). The LimFlow Crossing Stent Graft is indicated for patients who have chronic limb-threatening ischemia with no suitable endovascular or surgical revascularization options and are at risk of major amputation.

Limflow Inc.

Arteriovenous endovascular stent-graft

• Primary Device ID: 00850041730165
• NIH Device Record Key: 3125a811-ba94-433d-b74f-c557c65c7527
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LimFlow Crossing Stent Graft
• Version Model Number: RGS-35060-US-24
• Company DUNS: 096651686
• Company Name: Limflow Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850041730165 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P220025

FDA Product Code

• QWN: Stent Graft, Infrapopliteal, Venous Arterialization

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: 2024-10-16
• Device Publish Date: 2024-10-08

On-Brand Devices [LimFlow Crossing Stent Graft]

• 00850041730172: LimFlow Crossing Stent Graft (4.0-5.5 mm x 60 mm). The LimFlow Crossing Stent Graft is indicated
• 00850041730165: LimFlow Crossing Stent Graft (3.5-5.5 mm x 60 mm). The LimFlow Crossing Stent Graft is indicated