UDI device identifier
SURESIGN™ Digital Ovulation Rapid Test 01007-9
UDI device identifier 00045611010079 · Guangzhou Decheng Biotechnology Co., LTD
Key facts
| Primary DI | 00045611010079 |
|---|---|
| Brand name | SURESIGN™ Digital Ovulation Rapid Test |
| Version or model | 01007-9 |
| Company | Guangzhou Decheng Biotechnology Co., LTD |
| DUNS number | 554534314 |
| Product code | NGE |
| GMDN term | Luteinizing hormone (LH) IVD, kit, rapid ICT, self-testing |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jan 28, 2026 |
| Version date | Feb 5, 2026 |
| Description | 1ct Digital Ovulation Rapid Test Holder + 20ct Digital Ovulation Rapid Test Stick |
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: