Primary Device ID | 04250289503129 |
NIH Device Record Key | e0ec107f-fd7a-4157-bcd9-88ec201f93a4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AESKULISA tTg-A New Generation |
Version Model Number | 7503US |
Catalog Number | 7503US |
Company DUNS | 341714388 |
Company Name | Aesku.Diagnostics GmbH & Co. KG |
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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |