UDI device identifier
SURESIGN™ Menopause (FSH) Rapid Test 01005-5
UDI device identifier 00045611010055 · Guangzhou Decheng Biotechnology Co., LTD
Key facts
| Primary DI | 00045611010055 |
|---|---|
| Brand name | SURESIGN™ Menopause (FSH) Rapid Test |
| Version or model | 01005-5 |
| Company | Guangzhou Decheng Biotechnology Co., LTD |
| DUNS number | 554534314 |
| Product code | NGA |
| GMDN term | Follicle stimulating hormone (FSH) 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 | 2ct Menopause (FSH) Rapid Test |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 10–99 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: