UDI device identifier
Rite Aid 2T
UDI device identifier 00011822024419 · Guangzhou Decheng Biotechnology Co., LTD
Key facts
| Primary DI | 00011822024419 |
|---|---|
| Brand name | Rite Aid |
| Version or model | 2T |
| Company | Guangzhou Decheng Biotechnology Co., LTD |
| DUNS number | 554534314 |
| Product code | LCX |
| GMDN term | Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 27, 2024 |
| Version date | Oct 7, 2024 |
| Description | Rite Aid Pregnancy Tests, 1 Digital Pregnancy Rapid Test + 1 Early Detection Pregnancy Test, combo test kit |
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: