Primary Device ID | 00802526480928 |
NIH Device Record Key | f0d2fde9-d6db-46ef-b86c-b482019f549f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PUNCTUA™ CRT-D |
Version Model Number | N051 |
Company DUNS | 106295384 |
Company Name | BOSTON SCIENTIFIC CORPORATION |
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 | true |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | true |
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 | 00802526480928 [Primary] |
LWP | Implantable pulse generator, pacemaker (non-CRT) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2014-09-24 |
00802526480928 | Cardiac Resynchronization Therapy Defibrillator |
00802526480911 | Cardiac Resynchronization Therapy Defibrillator |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() PUNCTUA 76702688 4179595 Dead/Cancelled |
Cardiac Pacemakers, Inc. 2010-04-28 |