Primary Device ID | 00810050861809 |
NIH Device Record Key | 04ef3cb9-78b6-4fae-ba9b-8f81adab0bec |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Utility Pedestal Assembly |
Version Model Number | ST2-271-01-004 |
Company DUNS | 556196210 |
Company Name | LIFEPORT, LLC |
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 | false |