FDA UDI In Commercial Distribution 🇺🇸 United States

Number 1

DI: 00850040879162 · Model: NIT-1126-P · DEUS VULT, LLC
Product Codes
11
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Number 1
Primary DI
00850040879162
Version / Model
NIT-1126-P
Catalog Number
NIT-1126-P
Company Name
DEUS VULT, LLC
Labeler DUNS
086645029
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-01
Public Version
1
Public Version Date
2024-02-09
Public Version Status
New
Public Device Record Key
be5a8261-416b-4838-814c-ac77681f8fe5

Device Description

12-Panel Drug Test Cup: AMP, BZO, BUP, COC, MET, MTD, MDMA, OPI, OXY, PCP, TCA, THC

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
DKZ Enzyme Immunoassay, Amphetamine
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites
DIS Enzyme Immunoassay, Barbiturate
JXM Enzyme Immunoassay, Benzodiazepine
DJC Thin Layer Chromatography, Methamphetamine
DJG Enzyme Immunoassay, Opiates
DJR Enzyme Immunoassay, Methadone
LCM Enzyme Immunoassay, Phencyclidine
LFG Radioimmunoassay, Tricyclic Antidepressant Drugs
JXN Enzyme Immunoassay, Propoxyphene

GMDN Terms

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

Identifiers

Type ID
Primary 00850040879162
Package 00850040879179
Package 00850040879186

Customer Contacts

Phone
866-876-6355

Premarket Submissions

Submission Number Supplement Number
K131811 000