Primary Device ID | 04250289500463 |
NIH Device Record Key | 742a0acf-095b-4aac-80ba-b02a7b30ef1f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AESKULISA® U1-70 |
Version Model Number | 3104 |
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 | true |
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 |
Storage Environment Temperature | Between 2 Degrees Celsius and 8 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04250289500463 [Primary] |
LJM | Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-27 |
04250289502948 | AESKULISA U1-70 is a solid phase enzyme immunoassay employing recombinant human 70 kDa protein o |
04250289500463 | AESKULISA U1-70 is a solid phase enzyme immunoassay employing recombinant human 70 kDa protein o |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
AESKULISA 76374617 2878292 Live/Registered |
Matthias, Torsten 2002-02-22 |