ATAKR® II

GUDID 00721902257575

GENERATR 480201L ATAKR II RF 60W US LOAN

MEDTRONIC, INC.

Cardiac radio-frequency ablation system generator
Primary Device ID00721902257575
NIH Device Record Keyd6a0181e-1307-4a53-8e75-a24ff337de47
Commercial Distribution Discontinuation2018-06-21
Commercial Distribution StatusNot in Commercial Distribution
Brand NameATAKR® II
Version Model Number480201L
Company DUNS006261481
Company NameMEDTRONIC, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100721902257575 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LPBCardiac ablation percutaneous catheter

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2019-11-27
Device Publish Date2017-08-24

Devices Manufactured by MEDTRONIC, INC.

00763000613617 - Mosaic™7308C2025-03-11 SIZERS 7308C MOSAIC CINCH AORTIC MDR
00763000613624 - Mosaic Ultra™7308U2025-03-11 SIZERS 7308U MOSAIC ULTRA AORTIC MDR
00763000613631 - Mosaic™73102025-03-11 OBTURATORS 7310 MOSAIC MITRAL MDR
00763000613648 - NA2025-03-11 HANDLE 7639 VALVE MDR
00763000613655 - NA2025-03-11 HANDLE 7639XL VALVE XL MDR
00763000613662 - NA2025-03-11 ACCESSORY 7642 LOCK NUT MDR
00763000614034 - Hancock™ II 75052025-03-11 OBTURATOR 7505SET HK II AORTIC MDR
00763000614041 - Hancock™ II 75102025-03-11 OBTURATOR 7510SET HK II MITRAL MDR

Trademark Results [ATAKR]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ATAKR
ATAKR
85917318 not registered Dead/Abandoned
Medtronic, Inc.
2013-04-29
ATAKR
ATAKR
74251595 1788831 Dead/Cancelled
CardioRhythm
1992-03-02

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