UDI device identifier
e.p.t. Early Pregnancy Test e.p.t. Analog
UDI device identifier 00045611953031 · Nfi Consumer Products
Key facts
| Primary DI | 00045611953031 |
|---|---|
| Brand name | e.p.t. Early Pregnancy Test |
| Version or model | e.p.t. Analog |
| Company | Nfi Consumer Products |
| DUNS number | 016785052 |
| Product code | LCX |
| GMDN term | Total human chorionic gonadotropin IVD, kit, enzyme immunoassay (EIA) |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Nov 28, 2017 |
| Version date | Jul 6, 2023 |
| Description | ept analog 3 Ct |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 100–999 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: