LIAISON Q.S.E.T. Device Plus

GUDID 08056771602884

Fecal extraction device

Diasorin Inc.

Calprotectin IVD, reagent Calprotectin IVD, reagent Calprotectin IVD, reagent Calprotectin IVD, reagent Calprotectin IVD, reagent Calprotectin IVD, reagent Calprotectin IVD, reagent Calprotectin IVD, reagent Calprotectin IVD, reagent Calprotectin IVD, reagent Calprotectin IVD, reagent Calprotectin IVD, reagent
Primary Device ID08056771602884
NIH Device Record Key137cca98-5846-4fec-bbb2-a01a52db8d9e
Commercial Distribution StatusIn Commercial Distribution
Brand NameLIAISON Q.S.E.T. Device Plus
Version Model Number319060
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 Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108056771602884 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NXOCalprotectin, Fecal

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-08-17
Device Publish Date2022-08-09

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08056771602884 - LIAISON Q.S.E.T. Device Plus2022-08-17Fecal extraction device
08056771602884 - LIAISON Q.S.E.T. Device Plus2022-08-17 Fecal extraction device
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