| 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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