Primary Device ID | 08056771602952 |
NIH Device Record Key | e205cf0e-f0bf-4c95-a125-b44f77e68a63 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LIAISON Control QUANTIferon TB Gold Plus |
Version Model Number | 311021 |
Company DUNS | 033429783 |
Company Name | Diasorin Inc. |
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 | 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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08056771602952 [Primary] |
NCD | Test, Immunity, Cell Mediated, Mycobacterium Tuberculosis |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-09-18 |
Device Publish Date | 2023-09-08 |
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