UDI device identifier
TRUE METRIX GO HEB TRUE METRIX GO Self Monitoring Blood Glucose Meter Kit
UDI device identifier 00041220136131 · TRIVIDIA HEALTH, INC.
Key facts
| Primary DI | 00041220136131 |
|---|---|
| Brand name | TRUE METRIX GO |
| Version or model | HEB TRUE METRIX GO Self Monitoring Blood Glucose Meter Kit |
| Catalog number | RF4031-01 |
| Company | TRIVIDIA HEALTH, INC. |
| DUNS number | 151810868 |
| Product code | LFR |
| GMDN term | Glucose monitoring system IVD, home-use |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Feb 24, 2017 |
| Version date | Jun 9, 2025 |
| Description | HEB TRUE METRIX GO Self Monitoring Blood Glucose Meter Kit |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 100–999 GUDID devices with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About UDI device identifiers (GUDID)
The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.
Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date: