Primary Device ID | E312WC0112101 |
NIH Device Record Key | d49cde55-4f0b-46b9-b553-b153205f2195 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EDENTA |
Version Model Number | WC01-12 |
Company DUNS | 448002915 |
Company Name | EDENTA ETABLISSEMENT |
Device Count | 12 |
DM Exempt | true |
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 | true |
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 |