True Metrix Go
by Trividia Health, Inc. 10 variants
True Metrix Go (RF4031-01) is a Class II device made by Trividia Health, Inc., listed in FDA GUDID since 24 Feb 2017 (UDI-DI 00041220136131), registry data as of 19 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00041220136131 | Date24 Feb 2017 | StatusListed |
Official records
- AccessGUDID record 00041220136131
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Glucose monitoring system IVD, home-use
- Model / Ref / Catalog
- HEB TRUE METRIX GO Self Monitoring Blood Glucose Meter Kit, RF4031-01
- Primary DI / UDI-DI
- 00041220136131
- FDA product code
- LFR, NBW
- GMDN term
- Glucose monitoring system IVD, home-use
- Device class
- Class II
- Regulation number
- 862.1345
- GUDID distribution status
- In Commercial Distribution
From the manufacturer
Manufacturer's product page: TRUE METRIX®
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