FDA UDI In Commercial Distribution 🇺🇸 United States

MEDTOX® OXYCODONE

DI: 00690286000322 · Model: 601675 · MEDTOX DIAGNOSTICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MEDTOX® OXYCODONE
Primary DI
00690286000322
Version / Model
601675
Company Name
MEDTOX DIAGNOSTICS, INC.
Labeler DUNS
137417965
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
4
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
1aa21b42-a734-4b12-8218-4d3f63cb6112

Device Description

A qualitative one-step immunochromatographic test for the detection of Oxycodone and/or metabolites in human urine.

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
DJG Enzyme Immunoassay, Opiates

GMDN Terms

Code Name
55734 Oxycodone IVD, kit, rapid ICT, clinical

Identifiers

Type ID
Package 10690286000329
Primary 00690286000322

Customer Contacts

Phone
877-643-5703

Premarket Submissions

Submission Number Supplement Number
K060351 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 25 Degrees Celsius