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 |
00763000812065 - NA | 2024-03-19 WRENCH KIT 5873W TORQUE STERILE MDR |
00763000812072 - NA | 2024-03-19 TOOL 6056 PINCH ON AND FIX MDR |
20763000935584 - NA | 2024-03-19 CUSTOM PACK 12F72R 10PK R-PRIME |
20763000935607 - NA | 2024-03-19 CUSTOM PACK CB12D53R1 10PK 1/4 BRIDGE |
00763000940027 - NA | 2024-03-19 CUSTOM PACK 11X43R4 180028 |
00643169983229 - Avalus™ | 2024-03-18 VALVE 40029 AVALUS AOR MMX U30 US |
00763000757199 - NanoCross™ Elite | 2024-03-18 PTA AB14W015020090 NANOCROSS 014 V06 |
00763000757205 - NanoCross™ Elite | 2024-03-18 PTA AB14W015020150 NANOCROSS 014 V06 |
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 |