Primary Device ID | 00747252031405 |
NIH Device Record Key | ea7b5342-d0ef-434f-b0f7-2ff0ec70aca6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Superior Products Inc |
Version Model Number | MFY-960-8H-UP |
Company DUNS | 078607495 |
Company Name | Superior Products, 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 | true |
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 | false |