Primary Device ID | 00863095000108 |
NIH Device Record Key | c40ada15-4f50-47d1-9ea6-f1ac59e17bf0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Medstorm Defibrillator Pad |
Version Model Number | T100-CS |
Catalog Number | 16382 |
Company DUNS | 070556204 |
Company Name | BOUND TREE MEDICAL, LLC |
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 | true |
Serial Number | true |
Manufacturing Date | true |
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 | 00863095000108 [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 | 2014-11-07 |
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