FDA device listing
ALWAYS ALLDAYS PANTILINERS,Always menstrual pads,ALWAYS MENSTRUAL PADS,ALWAYS PADS,Always pantiliners
FDA device listing 1360976666 · PROCTER & GAMBLE GMBH
Key facts
| Proprietary names | ALWAYS ALLDAYS PANTILINERS,Always menstrual pads,ALWAYS MENSTRUAL PADS,ALWAYS PADS,Always pantiliners |
|---|---|
| Owner/operator | PROCTER & GAMBLE GMBH |
| Owner/operator number | 9004955 |
| Product codes | HHD |
| Device names | HHD - Pad, Menstrual, Unscented |
| Device class | Class I |
| Classification regulations (21 CFR) | 884.5435 |
| Review panels | Obstetrics/Gynecology |
| Registered establishments | PROCTER & GAMBLE GMBH & CO. MANUFACTURING OHE |
| Establishment registrations | 9680085 |
| FEI numbers | 3001116885 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database