ATAKR® II

GUDID 00721902257575

GENERATR 480201L ATAKR II RF 60W US LOAN

MEDTRONIC, INC.

Cardiac radio-frequency ablation system generator

• Primary Device ID: 00721902257575
• NIH Device Record Key: d6a0181e-1307-4a53-8e75-a24ff337de47
• Commercial Distribution Discontinuation: 2018-06-21
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: ATAKR® II
• Version Model Number: 480201L
• Company DUNS: 006261481
• Company Name: MEDTRONIC, 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• 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

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
• 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
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00721902257575 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P930029

FDA Product Code

• LPB: Cardiac ablation percutaneous catheter

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-11-27
• Device Publish Date: 2017-08-24

Devices Manufactured by MEDTRONIC, INC.

• 00763000613617 - Mosaic™7308C: 2025-03-11 SIZERS 7308C MOSAIC CINCH AORTIC MDR
• 00763000613624 - Mosaic Ultra™7308U: 2025-03-11 SIZERS 7308U MOSAIC ULTRA AORTIC MDR
• 00763000613631 - Mosaic™7310: 2025-03-11 OBTURATORS 7310 MOSAIC MITRAL MDR
• 00763000613648 - NA: 2025-03-11 HANDLE 7639 VALVE MDR
• 00763000613655 - NA: 2025-03-11 HANDLE 7639XL VALVE XL MDR
• 00763000613662 - NA: 2025-03-11 ACCESSORY 7642 LOCK NUT MDR
• 00763000614034 - Hancock™ II 7505: 2025-03-11 OBTURATOR 7505SET HK II AORTIC MDR
• 00763000614041 - Hancock™ II 7510: 2025-03-11 OBTURATOR 7510SET HK II MITRAL MDR