UDI device identifier
RITE AID BPAG1-20RITE
UDI device identifier 00011822589949 · MICROLIFE USA, INC.
Key facts
| Primary DI | 00011822589949 |
|---|---|
| Brand name | RITE AID |
| Version or model | BPAG1-20RITE |
| Company | MICROLIFE USA, INC. |
| DUNS number | 176387785 |
| Product code | DXQ |
| GMDN term | Aneroid manual sphygmomanometer |
| Premarket submission | K193259 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jan 7, 2022 |
| Version date | Jan 17, 2022 |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: