UDI device identifier
HealthMart One Step Pregnancy Test
UDI device identifier 00052569143803 · MCKESSON CORPORATION
Key facts
| Primary DI | 00052569143803 |
|---|---|
| Brand name | HealthMart |
| Version or model | One Step Pregnancy Test |
| Company | MCKESSON CORPORATION |
| DUNS number | 177667227 |
| Product code | LCX |
| GMDN term | Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical |
| Premarket submission | K042280 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Oct 2, 2020 |
| Version date | Jul 6, 2023 |
| Description | HealthMart SPS +/- Blue Cap |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: