UDI device identifier
The DivaCup Model A PL
UDI device identifier 00050428088852 · Diva International Inc
Key facts
| Primary DI | 00050428088852 |
|---|---|
| Brand name | The DivaCup |
| Version or model | Model A PL |
| Catalog number | 722537 |
| Company | Diva International Inc |
| DUNS number | 207651758 |
| Product code | HHE |
| GMDN term | Menstrual cup/disc, non-latex, reusable |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Mar 31, 2026 |
| Version date | Apr 8, 2026 |
| Description | Medical grade silicone, non-latex, soft reusable bell shape cup placed by the user into the vagina, held in place by suction and used to collect menstrual flow during menstruation in lieu of absorbent pads or tampons. It is available OTC (Over the counter). It is removed from the vagina by releasing… |
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: