LIAISON Lyme Total Antibody Plus Control set

GUDID 08056771602716

Diasorin Inc.

Borrelia burgdorferi immunoglobulin G (IgG)/IgM antibody IVD, control
Primary Device ID08056771602716
NIH Device Record Key92329742-894a-4d86-a09c-4cda75e32284
Commercial Distribution StatusIn Commercial Distribution
Brand NameLIAISON Lyme Total Antibody Plus Control set
Version Model Number318331
Company DUNS033429783
Company NameDiasorin Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108056771602716 [Primary]

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-02-11
Device Publish Date2020-02-03

Devices Manufactured by Diasorin Inc.

08056771602945 - LIAISON QUANTIferon TB Gold Plus2023-09-18 USA manufactured kit
08056771602952 - LIAISON Control QUANTIferon TB Gold Plus2023-09-18 USA manufactured control kit
08056771600002 - LIAISON® Testosterone2023-05-03
08056771600019 - LIAISON® Testosterone Control Set2023-05-03
08056771602969 - LIAISON MeMed BV2022-08-18 The DiaSorin LIAISON MeMed BV is a semi-quantitative assay that uses chemiluminescent immunoassay (CLIA) technology to measure
08056771602976 - LIAISON MeMed BV Control Set2022-08-18 The DiaSorin LIAISON MeMed BV Control Set is intended for use as assayed quality control samples to monitor the performance of t
08056771602884 - LIAISON Q.S.E.T. Device Plus2022-08-17 Fecal extraction device
08056771600590 - LIAISON Calprotectin 2022-06-10

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.