UDI device identifier
Kroger AT 0270KRO
UDI device identifier 00041260007804 · KROGER CO., THE
Key facts
| Primary DI | 00041260007804 |
|---|---|
| Brand name | Kroger |
| Version or model | AT 0270KRO |
| Company | KROGER CO., THE |
| DUNS number | 006999528 |
| Product code | FMK |
| GMDN term | Manual blood lancing device, reusable |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jun 11, 2021 |
| Version date | Jun 21, 2021 |
| Description | Kroger Autolet Lancing Device |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ 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: