FDA device listing
Medline Body Fluid Clean Up Kit
FDA device listing 1753036943 · Medline Industries, LP
Key facts
| Proprietary names | Medline Body Fluid Clean Up Kit |
|---|---|
| Owner/operator | Medline Industries, LP |
| Owner/operator number | 1417592 |
| Product codes | OKG |
| Device names | OKG - Body Fluid Clean Up Kit |
| Device class | Class II |
| Classification regulations (21 CFR) | 878.4040 |
| Review panels | General & Plastic Surgery |
| Registered establishments | Medline Industries, LP - Mexicali (MXC), Medline Soluciones Medicas, Nuevo Laredo Directo al Cliente, PRODUCTOS MEDLINE S.A. DE C.V. |
| Establishment registrations | 3004122598, 3015173212, 3045816902, 3045816907 |
| FEI numbers | 3004122598, 3015173212, 3045816902, 3045816907 |
| Establishment operations | Contract Sterilizer, 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