FDA UDI In Commercial Distribution 🇺🇸 United States

OralTox

DI: B313OT808071 · Model: OT80807 · PREMIER BIOTECH, INC
Product Codes
7
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

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Basic Information

Brand Name
OralTox
Primary DI
B313OT808071
Version / Model
OT80807
Company Name
PREMIER BIOTECH, INC
Labeler DUNS
010118759
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2018-09-24
Public Version
5
Public Version Date
2025-10-02
Public Version Status
Update
Public Device Record Key
f8fb2e38-d8ea-42c4-aa99-232953a385c3

Device Description

8 Panel OralTox - AMP/COC/MET/MTD/OPI/OXY/PCP/THC

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
LDJ Enzyme Immunoassay, Cannabinoids
LCM Enzyme Immunoassay, Phencyclidine
DJG Enzyme Immunoassay, Opiates
DJR Enzyme Immunoassay, Methadone
DJC Thin Layer Chromatography, Methamphetamine
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites
DKZ Enzyme Immunoassay, Amphetamine

GMDN Terms

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

Identifiers

Type ID
Primary B313OT808071
Unit of Use B313OT808070

Premarket Submissions

Submission Number Supplement Number
K181305 000