FDA UDI In Commercial Distribution 🇺🇸 United States

DrugCheck

DI: B298705110 · Model: 70511 · Express Diagnostic Int'l, Inc.
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DrugCheck
Primary DI
B298705110
Version / Model
70511
Catalog Number
70511
Company Name
Express Diagnostic Int'l, Inc.
Labeler DUNS
015875273
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-31
Public Version
3
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
1f8dd7dd-4555-4315-b34d-e751a6a8b3b7

Device Description

DrugCheck NxScan OnSite Drug Test, AMP500-COC-OPI300-PCP-THC

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites
NFT Test, Amphetamine, Over The Counter

GMDN Terms

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

Identifiers

Type ID
Primary B298705110

Customer Contacts

Phone
507-526-3951

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
4 – 30 Degrees Celsius