Primary Device ID | 00884838082120 |
NIH Device Record Key | ae4c22f1-7d88-4a5c-a655-dfdb6e0fbb39 |
Commercial Distribution Discontinuation | 2018-06-12 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Lifeline Response App |
Version Model Number | 300000161311 |
Catalog Number | mSafe |
Company DUNS | 080030042 |
Company Name | Lifeline Systems Company |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
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 | false |
OTC Over-The-Counter | true |