Primary Device ID | 00850015110061 |
NIH Device Record Key | 18a119aa-3dd2-4c42-9c52-9e9e0ad9a404 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TNE |
Version Model Number | 7700 |
Company DUNS | 012072823 |
Company Name | TEMREX CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |