UDI device identifier
Rite Aid Pharmacy Family Planning Pregnancy Test One Step
UDI device identifier 00011822096973 · SPD SWISS PRECISION DIAGNOSTICS GMBH
Key facts
| Primary DI | 00011822096973 |
|---|---|
| Brand name | Rite Aid Pharmacy |
| Version or model | Family Planning Pregnancy Test One Step |
| Company | SPD SWISS PRECISION DIAGNOSTICS GMBH |
| DUNS number | 483609579 |
| 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 | Aug 24, 2016 |
| Version date | Jul 6, 2023 |
| Description | FPPL Rite Aid SPS +/- (ER) |
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: