Primary Device ID | 00802526587863 |
NIH Device Record Key | 5c7ef232-b2c0-4f21-94da-be39841d79fc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PERCIVA™ ICD VR |
Version Model Number | D400 |
Company DUNS | 106295384 |
Company Name | BOSTON SCIENTIFIC CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | 00802526587863 [Primary] |
LWS | Implantable cardioverter defibrillator (non-CRT) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-12-06 |
Device Publish Date | 2017-09-27 |
00802526587924 | Implantable Cardioverter Defibrillator VR |
00802526587863 | Implantable Cardioverter Defibrillator VR |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() PERCIVA 86961495 5454084 Live/Registered |
Cardiac Pacemakers, Inc. 2016-04-01 |