UDI device identifier
ACTH [Adrenocorticotropic Hormone] ELISA 7023
UDI device identifier 00083059070231 · BIOMERICA, INC.
Key facts
| Primary DI | 00083059070231 |
|---|---|
| Brand name | ACTH [Adrenocorticotropic Hormone] ELISA |
| Version or model | 7023 |
| Company | BIOMERICA, INC. |
| DUNS number | 067647321 |
| Product code | CKG |
| GMDN term | Adrenocorticotropic hormone (ACTH) IVD, kit, enzyme immunoassay (EIA) |
| Premarket submission | K982608 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jul 1, 2020 |
| Version date | Jul 9, 2020 |
| Description | The Biomerica ACTH ELISA is intended for the quantitative determination of ACTH (Adrenocorticotropic Hormone) in human plasma. This assay is intended for in vitro diagnostic use. |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- Yes EUDAMED counterpart found
- 10–99 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: