FDA UDI In Commercial Distribution 🇺🇸 United States

TRUEtrack

DI: 10021292006843 · Model: TRUEtrack PRE-PACK · TRIVIDIA HEALTH, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TRUEtrack
Primary DI
10021292006843
Version / Model
TRUEtrack PRE-PACK
Catalog Number
A4H01-75
Company Name
TRIVIDIA HEALTH, INC.
Labeler DUNS
151810868
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-20
Public Version
3
Public Version Date
2021-11-01
Public Version Status
Update
Public Device Record Key
3302fe9a-9939-4e40-9b76-7ea96d8b9c07

Device Description

TRUEtrack PRE-PACK

Device Characteristics

Single Use
No
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
CGA Glucose Oxidase, Glucose
NBW System, Test, Blood Glucose, Over The Counter
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

GMDN Terms

Code Name
62537 Glucose monitoring system IVD, home-use

Identifiers

Type ID
Primary 10021292006843

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K032657 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
40 – 86 Degrees Fahrenheit