DrugCheck 60619

GUDID B298606190

NxStep OnSite Drug Test, AMP-BARB-BZO-COC-OPI300-THC

Express Diagnostic Int'l, Inc.

Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Primary Device IDB298606190
NIH Device Record Key47551a04-f182-4a4b-8d1f-446e8785bc91
Commercial Distribution StatusIn Commercial Distribution
Brand NameDrugCheck
Version Model Number60619
Catalog Number60619
Company DUNS015875273
Company NameExpress Diagnostic Int'l, 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

Customer Support Contacts

Phone507-526-3951
Emailquality@drugcheck.com
Phone507-526-3951
Emailquality@drugcheck.com
Phone507-526-3951
Emailquality@drugcheck.com
Phone507-526-3951
Emailquality@drugcheck.com
Phone507-526-3951
Emailquality@drugcheck.com
Phone507-526-3951
Emailquality@drugcheck.com
Phone507-526-3951
Emailquality@drugcheck.com
Phone507-526-3951
Emailquality@drugcheck.com
Phone507-526-3951
Emailquality@drugcheck.com
Phone507-526-3951
Emailquality@drugcheck.com
Phone507-526-3951
Emailquality@drugcheck.com
Phone507-526-3951
Emailquality@drugcheck.com
Phone507-526-3951
Emailquality@drugcheck.com
Phone507-526-3951
Emailquality@drugcheck.com
Phone507-526-3951
Emailquality@drugcheck.com
Phone507-526-3951
Emailquality@drugcheck.com
Phone507-526-3951
Emailquality@drugcheck.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB298606190 [Primary]

FDA Product Code

DKZEnzyme Immunoassay, Amphetamine

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-04-24
Device Publish Date2023-04-14