GUDID 20885074489791

PK TL4J94R1 SET A, CYCLOHEX

MEDTRONIC, INC.

Cardiopulmonary bypass system tubing set Cardiopulmonary bypass system tubing set Cardiopulmonary bypass system blood tubing set Cardiopulmonary bypass system blood tubing set Cardiopulmonary bypass system blood tubing set Cardiopulmonary bypass system blood tubing set Cardiopulmonary bypass system blood tubing set Cardiopulmonary bypass system blood tubing set Cardiopulmonary bypass system blood tubing set Cardiopulmonary bypass system blood tubing set

• Primary Device ID: 20885074489791
• NIH Device Record Key: c5163a84-0703-4c45-a289-7741f3529479
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: TL4J94R1
• Company DUNS: 006261481
• Company Name: MEDTRONIC, INC.
• Device Count: 2
• 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: true
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885074489797 [Unit of Use]
GS1	20885074489791 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K800178

FDA Product Code

• DWE: TUBING, PUMP, 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: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-05-21

Devices Manufactured by MEDTRONIC, INC.

• 20763000770291 - TrailBlazer™: 2024-07-16 PS ASC-014-090 TRAILBLAZER ANGLED V04
• 20763000770307 - TrailBlazer™: 2024-07-16 PS ASC-014-135 TRAILBLAZER ANGLED V04
• 20763000770314 - TrailBlazer™: 2024-07-16 PS ASC-014-150 TRAILBLAZER ANGLED V04
• 20763000770321 - TrailBlazer™: 2024-07-16 PS ASC-018-090 TRAILBLAZER ANGLED V04
• 20763000770338 - TrailBlazer™: 2024-07-16 PS ASC-018-135 TRAILBLAZER ANGLED V04
• 20763000770345 - TrailBlazer™: 2024-07-16 PS ASC-018-150 TRAILBLAZER ANGLED V04
• 20763000770352 - TrailBlazer™: 2024-07-16 PS ASC-035-065 TRAILBLAZER ANGLED V04
• 20763000770369 - TrailBlazer™: 2024-07-16 PS ASC-035-090 TRAILBLAZER ANGLED V04