UDI device identifier
Tampax Tampax Cup
UDI device identifier 00073010715325 · PROCTER & GAMBLE MANUFACTURING COMPANY, THE
Key facts
| Primary DI | 00073010715325 |
|---|---|
| Brand name | Tampax |
| Version or model | Tampax Cup |
| Company | PROCTER & GAMBLE MANUFACTURING COMPANY, THE |
| DUNS number | 004238200 |
| 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 | Aug 30, 2021 |
| Version date | Jul 14, 2025 |
| Description | Tampax Cup Regular + Heavy 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: