Primary Device ID | 00840314800008 |
NIH Device Record Key | b9d840fb-afe2-4e24-8078-1b472d1d039f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PARALLEL BAR,FLR MTD,7'L HT&W ADJ(2P |
Version Model Number | 1389 |
Company DUNS | 001892660 |
Company Name | Hausmann Enterprises, 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 |