FDA UDI Not in Commercial Distribution 🇺🇸 United States

Preferred Med Supply

DI: 00860004081609 · Model: PF12P · DEUS VULT, LLC
Product Codes
12
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
Preferred Med Supply
Primary DI
00860004081609
Version / Model
PF12P
Catalog Number
PF12P
Company Name
DEUS VULT, LLC
Labeler DUNS
086645029
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-08-11
Public Version
3
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
3ad277b5-1210-4531-8f4c-bd6f5162fedf
Distribution End Date
2021-12-31

Device Description

Multi-panel Drug Test Cup

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QBF Test, Propoxyphene, Over The Counter
NFY Test, Cocaine And Cocaine Metabolites, Over The Counter
NGI Test, Morphine, Over The Counter
NGL Test, Opiates, Over The Counter
PTG Test, Methadone, Over The Counter
NGG Test, Methamphetamine, Over The Counter
NGM Test, Phencyclidine (Pcp), Over The Counter
PTH Test, Barbiturate, Over The Counter
QAW Test, Tricyclic Antidepressants, Over The Counter
NFT Test, Amphetamine, Over The Counter
NFW Test, Cannabinoid, Over The Counter
NFV Test, Benzodiazepine, Over The Counter

GMDN Terms

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

Identifiers

Type ID
Primary 00860004081609
Package 00860004081616
Package 00860004081623
Package 00860004081630

Customer Contacts

Phone
866-876-6355

Premarket Submissions

Submission Number Supplement Number
K182654 000