CRL Stat ™ KCUR920099

GUDID 00817815020990

DOA 5 in 1 Test CRL QuickScreen Cup W/AD, 25Pcs/Box; Without Security Label & No Disposable Gloves COC/mAMP/OPI/PCP/THC/PH-SG-OX CLIA waived

CLINICAL REFERENCE LABORATORY, INC.

Multiple drugs of abuse IVD, kit, immunochromatographic test (ICT), rapid
Primary Device ID00817815020990
NIH Device Record Key001e1006-8a0f-4159-98e3-21d091323510
Commercial Distribution StatusIn Commercial Distribution
Brand NameCRL Stat ™
Version Model NumberKCUR920099
Catalog NumberKCUR920099
Company DUNS098268311
Company NameCLINICAL REFERENCE LABORATORY, INC.
Device Count25
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
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
GS100817815020976 [Unit of Use]
GS100817815020990 [Primary]

FDA Product Code

DKEReagents, Test, Tetrahydrocannabinol

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-05-31
Device Publish Date2016-10-14

On-Brand Devices [CRL Stat ™]

00817815020990DOA 5 in 1 Test CRL QuickScreen Cup W/AD, 25Pcs/Box; Without Security Label & No Disposable Glov
00817815020983DOA 10 in 1 Test CRL QuickScreen Cup W/AD, 25Pcs/Box; Without Security Label & No Disposable Glo

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