Primary Device ID | 00884838084810 |
NIH Device Record Key | 9c13a83e-3f30-477a-bd76-22da865ecfd3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Philips GoSafe |
Version Model Number | 300000188981 |
Catalog Number | 7100MHB |
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 | true |
Manufacturing Date | true |
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 |