FlexFlow Venous Cannula

GUDID 10803622128100

LIVANOVA USA, INC.

Cardiopulmonary bypass cannula, femoral Cardiopulmonary bypass cannula, femoral

• Primary Device ID: 10803622128100
• NIH Device Record Key: 571d7e40-cabd-417a-bf01-162c9e2007a6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FlexFlow Venous Cannula
• Version Model Number: 200-200
• Company DUNS: 080914995
• Company Name: LIVANOVA USA, 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00803622128103 [Primary]
GS1	10803622128100 [Package]; Contains: 00803622128103; Package: CASE [1 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K052081

FDA Product Code

• DWF: CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS

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: 2018-08-15
• Device Publish Date: 2015-09-17

On-Brand Devices [FlexFlow Venous Cannula]

• 10803622128100: 200-200
• 10803622125819: 200-200
• 10803622147286: 200-200