UDI device identifier
SURESIGN™ Digital Pregnancy Rapid Test 01002-4
UDI device identifier 00045611010024 · Guangzhou Decheng Biotechnology Co., LTD
Key facts
| Primary DI | 00045611010024 |
|---|---|
| Brand name | SURESIGN™ Digital Pregnancy Rapid Test |
| Version or model | 01002-4 |
| Company | Guangzhou Decheng Biotechnology Co., LTD |
| DUNS number | 554534314 |
| Product code | LCX |
| GMDN term | Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical |
| Premarket submission | K222305 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jan 28, 2026 |
| Version date | Feb 5, 2026 |
| Description | 3ct 25mIU - Digital 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: