Primary Device ID | 00884838093638 |
NIH Device Record Key | 243d7df7-047e-4609-a960-1b1fc742bc9a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Philips GoSafe 2 |
Version Model Number | 300002706311 |
Catalog Number | 7250MHB |
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 |