FDA UDI Not in Commercial Distribution 🇺🇸 United States

VERDICT®-II

DI: 00690286000131 · Model: 601587 · MEDTOX DIAGNOSTICS, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
VERDICT®-II
Primary DI
00690286000131
Version / Model
601587
Company Name
MEDTOX DIAGNOSTICS, INC.
Labeler DUNS
137417965
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
7
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
e42b0ca6-e013-4d8e-b8a6-52ce7fce75ec
Distribution End Date
2020-07-31

Device Description

A qualitative one-step immunochromatographic test panel for the detection of Cannabinoids (THC) and Cocaine and/or their metabolites in human urine.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
Sterilization Prior Use
No

Product Codes

Code Name
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites
DKE Reagents, Test, Tetrahydrocannabinol

GMDN Terms

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

Identifiers

Type ID
Primary 00690286000131
Package 10690286000138

Customer Contacts

Phone
877-643-5703

Premarket Submissions

Submission Number Supplement Number
K003687 000
K982211 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 25 Degrees Celsius