CP5

GUDID 04033817900955

LivaNova Deutschland GmbH

Cardiopulmonary bypass system, roller type

• Primary Device ID: 04033817900955
• NIH Device Record Key: 53dbee35-bf50-4d04-b979-a956e7c991b9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CP5
• Version Model Number: Emergency System
• Company DUNS: 343225272
• Company Name: LivaNova Deutschland GmbH
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• 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	04033817900955 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K112225

FDA Product Code

• DWA: Control, pump speed, cardiopulmonary bypass

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2024-05-07
• Device Publish Date: 2015-10-20

On-Brand Devices [CP5]

• 04033817902782: Pump Control Panel
• 04033817901006: Pump Control Panel
• 04033817900955: Emergency System
• 04033817900948: Drive Unit