UDI device identifier
Myoglobin Enzyme Immunoassay Test Kit 7030
UDI device identifier 00083059070309 · BIOMERICA, INC.
Key facts
| Primary DI | 00083059070309 |
|---|---|
| Brand name | Myoglobin Enzyme Immunoassay Test Kit |
| Version or model | 7030 |
| Company | BIOMERICA, INC. |
| DUNS number | 067647321 |
| Product code | DRR |
| GMDN term | Myoglobin IVD, kit, enzyme immunoassay (EIA) |
| Premarket submission | K022660 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jul 1, 2020 |
| Version date | Jul 9, 2020 |
| Description | The Myoglobin ELISA is intended for the quantitative determination of myoglobin in human serum. |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 1–9 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: