FDA device listing
Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile
FDA device listing 1898738699 · KIMBERLY-CLARK CORPORATION
Key facts
| Owner/operator | KIMBERLY-CLARK CORPORATION |
|---|---|
| Owner/operator number | 9036574 |
| Product codes | NRC |
| Device names | NRC - Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile |
| Device class | Class I |
| Classification regulations (21 CFR) | 884.5425 |
| Review panels | Obstetrics/Gynecology |
| Registered establishments | KIMBERLY-CLARK PERSONAL HYGIENIC PRODUCTS CO.,LTD.BEIJING, KIMBERLY-CLARK PERSONAL HYGIENIC PRODUCTS, LTD. |
| Establishment registrations | 9615624, 9615625 |
| FEI numbers | 3005513666, 3043515936 |
| Establishment operations | Contract 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