Primary Device ID | 05415067029348 |
NIH Device Record Key | 5999d3ee-2597-4989-82be-b67e801f50a9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TactiSys™ Quartz Equipment |
Version Model Number | Mounting Bracket |
Catalog Number | TSM-BSD-GBL |
Company DUNS | 149818952 |
Company Name | ST. JUDE MEDICAL, 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 | true |
Serial Number | false |
Manufacturing Date | true |
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 |
Phone | +1(855)478-5833 |
customerservice@sjm.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05415067029348 [Primary] |
OAE | Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-10-12 |
05415067029355 | Tactisys to Precision Above Mounting Bracket |
05415067029348 | Tactisys to Precision Beside Mounting Bracket |
05415067034700 | TactiFlex Radiofrequency Cable |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() TACTISYS 85080190 3900774 Live/Registered |
ENDOSENSE SA 2010-07-08 |