UDI device identifier
My-TECH My-TECH Self Monitoring Blood Glucose Test Strips
UDI device identifier 00021292013127 · TRIVIDIA HEALTH, INC.
Key facts
| Primary DI | 00021292013127 |
|---|---|
| Brand name | My-TECH |
| Version or model | My-TECH Self Monitoring Blood Glucose Test Strips |
| Company | TRIVIDIA HEALTH, INC. |
| DUNS number | 151810868 |
| Product code | LFR |
| GMDN term | Glucose monitoring system IVD, home-use |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Aug 8, 2019 |
| Version date | Jun 9, 2025 |
| Description | My-TECH Self Monitoring Blood Glucose Test Strips |
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: