Primary Device ID | 00815871020008 |
NIH Device Record Key | e3fdacb6-f5d5-4b54-8bea-2c13894fe5df |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ASG 120 |
Version Model Number | 71250ASG |
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 | false |
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 |