FDA UDI In Commercial Distribution 🇺🇸 United States

MEDTOX®

DI: 00690286000629 · Model: 102368 · MEDTOX DIAGNOSTICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MEDTOX®
Primary DI
00690286000629
Version / Model
102368
Company Name
MEDTOX DIAGNOSTICS, INC.
Labeler DUNS
137417965
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
c95b2027-54de-47c8-8b0f-f75db87c80af

Device Description

Positive toxicology urine control used to monitor and validate the performance of MEDTOX® drugs of abuse test devices.

Device Characteristics

Single Use
No
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
DIF Drug Mixture Control Materials

GMDN Terms

Code Name
55461 Multiple drugs of abuse IVD, control

Identifiers

Type ID
Primary 00690286000629

Customer Contacts

Phone
877-643-5703

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-20 – 8 Degrees Celsius