Primary Device ID | 00815871020367 |
NIH Device Record Key | 697c8c47-6642-431e-ad28-d8a281b8be69 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | E-ST |
Version Model Number | 60132 |
Company DUNS | 178440426 |
Company Name | Avante |
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 | false |
Lot Batch | false |
Serial Number | true |
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 |