LimFlow V-Ceiver

GUDID 00850041730004

The LimFlow V-Ceiver is intended for use in the cardiovascular system to manipulate and retrieve guidewires specified in the IFU.

Limflow Inc.

Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare

• Primary Device ID: 00850041730004
• NIH Device Record Key: 7674acbf-ee7c-4a46-925f-3610442c3baf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LimFlow V-Ceiver
• Version Model Number: VC-US-21
• 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: true
• 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
• Phone: 18884787705
• Email: info@limflow.com
• Phone: 18884787705
• Email: info@limflow.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850041730004 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K222083

FDA Product Code

• MMX: Device, Percutaneous Retrieval

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: 2023-07-04
• Device Publish Date: 2023-06-26

On-Brand Devices [LimFlow V-Ceiver]

• 00850041730004: The LimFlow V-Ceiver is intended for use in the cardiovascular system to manipulate and retrieve
• 00850041730141: The LimFlow V-Ceiver is intended for use in the cardiovascular system to manipulate and retrieve