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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00721902257575 [Primary] |
LPB | Cardiac ablation percutaneous catheter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2019-11-27 |
Device Publish Date | 2017-08-24 |
00199150025381 - NA | 2025-06-27 CUSTOM PACK BB11P25R3 VCH CENT V A |
20199150025521 - NA | 2025-06-27 CUSTOM PACK BB9G37R2 5PK L VD AC |
00199150026326 - NA | 2025-06-27 CUSTOM PACK BB11Z33R8 ALINA CPB |
00199150026579 - NA | 2025-06-27 CUSTOM PACK BB5722R48 CHRT INF |
00199150026692 - NA | 2025-06-27 CUSTOM PACK BB8R73R14 NH ADULT PACK |
00199150026715 - NA | 2025-06-27 CUSTOM PACK BB6M71R12 CP PRIME |
00199150026746 - NA | 2025-06-27 CUSTOM PACK BB7A25R12 PED |
00199150026753 - NA | 2025-06-27 CUSTOM PACK BB12E34R4 SUPPORT PACK |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() ATAKR 85917318 not registered Dead/Abandoned |
Medtronic, Inc. 2013-04-29 |
![]() ATAKR 74251595 1788831 Dead/Cancelled |
CardioRhythm 1992-03-02 |