UDI device identifier
EZ-GIARDIA One-Step Giardia Test 1501-15
UDI device identifier 00083059150155 · BIOMERICA, INC.
Key facts
| Primary DI | 00083059150155 |
|---|---|
| Brand name | EZ-GIARDIA One-Step Giardia Test |
| Version or model | 1501-15 |
| Company | BIOMERICA, INC. |
| DUNS number | 067647321 |
| Product code | MHI |
| GMDN term | Giardia lamblia antigen IVD, kit, enzyme immunoassay (EIA) |
| 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 Giardia test is a rapid chromatographic immunoassay for the qualitative detection of Giardia antigens in human stool samples. The In Vitro test is intended for professional use only. |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No 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: