FDA UDI In Commercial Distribution 🇺🇸 United States

UCP Home Drug Screening Test Cards

DI: 10817038020491 · Model: U-DOA-3124 · UCP BIOSCIENCES, INC.
Product Codes
10
GMDN Terms
1
Identifiers
3
Pkg Device Count
25

Basic Information

Brand Name
UCP Home Drug Screening Test Cards
Primary DI
10817038020491
Version / Model
U-DOA-3124
Catalog Number
U-DOA-3124
Company Name
UCP BIOSCIENCES, INC.
Labeler DUNS
163610020
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
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
bf7760de-3c04-4c6c-b27c-4c5babfa53f1

Device Description

12 Panel Drug Test Card BZO/BAR/COC/THC/mAMP/MOP/MTD/TCA/OXY/MDMA/PCP/AMP

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
DKZ Enzyme Immunoassay, Amphetamine
LCM Enzyme Immunoassay, Phencyclidine
LFG Radioimmunoassay, Tricyclic Antidepressant Drugs
DJR Enzyme Immunoassay, Methadone
DJG Enzyme Immunoassay, Opiates
DJC Thin Layer Chromatography, Methamphetamine
LDJ Enzyme Immunoassay, Cannabinoids
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites
DIS Enzyme Immunoassay, Barbiturate
JXM Enzyme Immunoassay, Benzodiazepine

GMDN Terms

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

Identifiers

Type ID
Package 20817038020498
Primary 10817038020491
Unit of Use 00817038020494

Premarket Submissions

Submission Number Supplement Number
K050540 000
K130463 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 30 Degrees Celsius