FDA device listing
AMD-Ritmed Cotton Roll,AMD-Ritmed Dressing,AMD-Ritmed Fine Gauze Mesh,AMD-Ritmed Fluff Sponge,AMD-Ritmed…
FDA device listing 1575431524 · Medicom Group
Key facts
| Proprietary names | AMD-Ritmed Cotton Roll,AMD-Ritmed Dressing,AMD-Ritmed Fine Gauze Mesh,AMD-Ritmed Fluff Sponge,AMD-Ritmed Gauze,AMD-Ritmed Gauze Bandage,AMD-Ritmed Gauze Roll,AMD-Ritmed Gauze Sponge,AMD-Ritmed Krimped Bandage,AMD-Ritmed Non-Adherent Pad,AMD-Ritmed O.R. Towel,AMD-Ritmed Pad,AMD-Ritmed Sponge,AMD-Ritmed Stick Sponge,Dermafill Biocellulose Dressing,Medicom Gauze Sponge,Medicom Non-Woven Sponge |
|---|---|
| Owner/operator | Medicom Group |
| Owner/operator number | 8020405 |
| Product codes | NAC |
| Device names | NAC - Dressing, Wound, Hydrophilic |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4018 |
| Review panels | General & Plastic Surgery |
| Registered establishments | AMD Medicom Inc. |
| Establishment registrations | 9611959 |
| FEI numbers | 3002677549 |
| Establishment operations | Complaint File Establishment, Foreign Exporter, Specification Developer |
| 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