Primary Device ID | 00812394020133 |
NIH Device Record Key | 237870f5-c390-4c23-9cca-9309d67574a0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Intellisense® Battery Powerheart® G5 |
Version Model Number | XBTAED001A |
Catalog Number | XBTAED001A |
Company DUNS | 190713797 |
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 |
Phone | +1.262.953.3500 |
techsupport@cardiacscience.com | |
Phone | +1.262.953.3500 |
techsupport@cardiacscience.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00812394020133 [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 | 2015-04-29 |
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