RECOVERY CONE® FBRC

GUDID 00801741040948

RECOVERY CONE® Removal System

Bard Peripheral Vascular, Inc.

Vena cava filter extraction/repositioning kit

• Primary Device ID: 00801741040948
• NIH Device Record Key: e29c5971-2627-44b4-b952-71b52835b395
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RECOVERY CONE®
• Version Model Number: FBRC
• Catalog Number: FBRC
• Company DUNS: 135057938
• Company Name: Bard Peripheral Vascular, 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: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741040948 [Primary]

FDA Product Code

• MMX: Device, percutaneous retrieval

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-19

On-Brand Devices [RECOVERY CONE®]

• 00801741040948: RECOVERY CONE® Removal System
• 00801741040931: RECOVERY CONE® Removal System