Primary Device ID | 00840314803603 |
NIH Device Record Key | d3ced145-ba6c-4f9b-b647-e13c35b1b7e0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HTT,78X30,OAK,PF Black,A07,A09,A03 |
Version Model Number | HTT-3078-L01V23-A09A07A03 |
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 |