LimFlow Vector

GUDID 00850041730134

The LimFlow Vector is intended for the treatment of vascular disorders and more particularly for excising or disrupting venous valves

Limflow Inc.

Valvulotome, percutaneous

• Primary Device ID: 00850041730134
• NIH Device Record Key: 602dcf4b-048b-425d-84ad-fa86c88c6db9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LimFlow Vector
• Version Model Number: VT-US-23
• Company DUNS: 096651686
• Company Name: Limflow 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850041730134 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K221902

FDA Product Code

• MGZ: Valvulotome

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: 2024-04-22
• Device Publish Date: 2024-04-12

On-Brand Devices [LimFlow Vector]

• 00850041730028: The LimFlow Vector is intended for the treatment of vascular disorders and more particularly for
• 00850041730134: The LimFlow Vector is intended for the treatment of vascular disorders and more particularly for