UDI device identifier
Family Wellness Early Result Pregnancy Test PLPL
UDI device identifier 00032251060748 · SPD SWISS PRECISION DIAGNOSTICS GMBH
Key facts
| Primary DI | 00032251060748 |
|---|---|
| Brand name | Family Wellness Early Result Pregnancy Test |
| Version or model | PLPL |
| 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 | Jun 30, 2016 |
| Version date | Jul 6, 2023 |
| Description | Family Wellness Early Result Pregnancy Test |
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: