CENTRIMAG® BACK-UP CONSOLE WITH BATTERIES 201-90200

GUDID 07640135140870

BACK-UP CONSOLE WITH BATTERIES

Thoratec Switzerland GmbH

Cardiopulmonary bypass system centrifugal pump backup drive unit

• Primary Device ID: 07640135140870
• NIH Device Record Key: 3531b067-3bb4-4248-aced-832da0d13200
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CENTRIMAG® BACK-UP CONSOLE WITH BATTERIES
• Version Model Number: 201-90200
• Catalog Number: 201-90200
• Company DUNS: 486066918
• Company Name: Thoratec Switzerland 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: 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(855)478-5833
• Email: customerservice@sjm.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640135140870 [Primary]

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: 5
• Public Version Date: 2019-02-06
• Device Publish Date: 2014-09-20

On-Brand Devices [CENTRIMAG® BACK-UP CONSOLE WITH BATTERIES]

• 07640135140887: BACK-UP CONSOLE WITH BATTERIES
• 07640135140870: BACK-UP CONSOLE WITH BATTERIES
• 07640135140863: Back-Up Console with Batteries