Primary Device ID | 00812394020867 |
NIH Device Record Key | 6c67d3b7-b873-4449-92e2-5a4d21dd6f8a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Powerheart® Pro Battery |
Version Model Number | 9145-301 |
Catalog Number | 9145-301 |
Company DUNS | 080355564 |
Company Name | CARDIAC SCIENCE 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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00812394020119 [Previous] |
GS1 | 00812394020867 [Primary] |
MKJ | Automated External Defibrillators (Non-Wearable) |
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 | 2017-02-10 |
00812394020867 | IntelliSense lithium battery: For Powerheart® G3 Pro model 9300P with 1 year full replacement g |
00812394020119 | 9145-301 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
POWERHEART 78905168 3206323 Live/Registered |
CARDIAC SCIENCE CORPORATION 2006-06-09 |
POWERHEART 77687247 not registered Dead/Abandoned |
Hunter Laboratories, Inc. 2009-03-10 |
POWERHEART 74367566 1955504 Live/Registered |
CARDIAC SCIENCE CORPORATION 1993-03-12 |