Abiomed Breethe OXY-1 System

GUDID 00813502013245

Tubing, Translucent Green, 1/4" x 3/8"

Breethe, Inc.

Cardiopulmonary bypass system, non-roller type

• Primary Device ID: 00813502013245
• NIH Device Record Key: 639dfced-06bf-45ec-ade2-60a0ac4de3e1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Abiomed Breethe OXY-1 System
• Version Model Number: 3001030
• Company DUNS: 079455574
• Company Name: Breethe, 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	00813502013245 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K223161

FDA Product Code

• DTZ: Oxygenator, Cardiopulmonary Bypass

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: 2023-06-12
• Device Publish Date: 2023-06-02

On-Brand Devices [Abiomed Breethe OXY-1 System]

• 00860001797985: OXY-1 US Power Cord 3M Qty 1
• 00813502012361: OXY-1 Console Intake Filter Qty 5
• 00813502012354: OXY-1 Condensate Tray Qty 5
• 00813502013245: Tubing, Translucent Green, 1/4" x 3/8"
• 00813502013184: TUBING INSULATOR KIT