Primary Device ID | 00802526062568 |
NIH Device Record Key | bd91303f-0850-4bd5-bb8b-a34c51722da9 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 2902 |
Company DUNS | 106295384 |
Company Name | BOSTON SCIENTIFIC CORPORATION |
Device Count | 1 |
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 | 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 | 00802526062568 [Primary] |
LWS | Implantable cardioverter defibrillator (non-CRT) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2014-09-24 |
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