FDA UDI Not in Commercial Distribution 🇺🇸 United States

TRUE METRIX GO

DI: 00021292009335 · Model: TRUE METRIX GO Self Monitoring Blood Glucose Meter · TRIVIDIA HEALTH, INC.
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
TRUE METRIX GO
Primary DI
00021292009335
Version / Model
TRUE METRIX GO Self Monitoring Blood Glucose Meter
Catalog Number
RF4023-01
Company Name
TRIVIDIA HEALTH, INC.
Labeler DUNS
151810868
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-01-18
Public Version
5
Public Version Date
2023-10-16
Public Version Status
Update
Public Device Record Key
06f48915-4239-46da-bc0b-0ac1c3b379a0
Distribution End Date
2020-06-02

Device Description

Fred's TRUE METRIX GO Self Monitoring Blood Glucose Meter Kit box

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
Yes
Kit
Yes
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
Yes
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
LFR Glucose Dehydrogenase, Glucose
NBW System, Test, Blood Glucose, Over The Counter

GMDN Terms

Code Name
62537 Glucose monitoring system IVD, home-use

Identifiers

Type ID
Package 10021292009332
Primary 00021292009335
Direct Marking 00021292007706

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K143548 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
40 – 86 Degrees Fahrenheit