FDA UDI Not in Commercial Distribution 🇺🇸 United States

DrugCheck

DI: B2983097050 · Model: 30970-5 · EXPRESS DIAGNOSTICS INT'L, INC.
Product Codes
7
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DrugCheck
Primary DI
B2983097050
Version / Model
30970-5
Catalog Number
30970-5
Company Name
EXPRESS DIAGNOSTICS INT'L, INC.
Labeler DUNS
168560402
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-30
Public Version
5
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
e1aeebf7-d40d-4580-a002-a1b1430cdbcc
Distribution End Date
2019-04-26

Device Description

9 Panel Dip Drug Test, AMP-BUP-BZO-COC-MET-MTD-OPI300-OXY-THC-pH,SG,OX-CR,NI

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LDJ Enzyme Immunoassay, Cannabinoids
DJR Enzyme Immunoassay, Methadone
LAF Gas Chromatography, Methamphetamine
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites
JXM Enzyme Immunoassay, Benzodiazepine
DJG Enzyme Immunoassay, Opiates
DKZ Enzyme Immunoassay, Amphetamine

GMDN Terms

Code Name
46994 Multiple drugs of abuse IVD, kit, rapid ICT, clinical

Identifiers

Type ID
Primary B2983097050

Customer Contacts

Phone
507-526-3951

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 30 Degrees Celsius