QuikStrip Multidrug Screening Dip Card Test

GUDID 20748349000377

QuikStrip Multidrug 5 Test, AMP 500, COC 300, MET 500, OP I 2000, THC 50

SYNTRON BIORESEARCH, INC.

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Primary Device ID20748349000377
NIH Device Record Keyb4545dd6-0da8-4670-9d69-00b19e472277
Commercial Distribution StatusIn Commercial Distribution
Brand NameQuikStrip Multidrug Screening Dip Card Test
Version Model Number30500
Company DUNS174517060
Company NameSYNTRON BIORESEARCH, 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 Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100748349000373 [Primary]
GS110748349000370 [Package]
Contains: 00748349000373
Package: Kit Box [25 Units]
In Commercial Distribution
GS120748349000377 [Package]
Contains: 10748349000370
Package: Shipper Box [4 Units]
In Commercial Distribution

FDA Product Code

LDJEnzyme Immunoassay, Cannabinoids

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-06-05

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