Primary Device ID | 00817051022871 |
NIH Device Record Key | ee720065-4235-4534-a06e-17a0f22f08b6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EZ |
Version Model Number | 914040 |
Company DUNS | 053707303 |
Company Name | CENTRIX, INC. |
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 | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |