Primary Device ID | 00816795024318 |
NIH Device Record Key | d3d70a9a-495e-4d96-bbf5-0693b9748901 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Delta Zirconia Anterior |
Version Model Number | D814A0ANT |
Company DUNS | 030580955 |
Company Name | AURIDENT INC |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |