FDA device listing
ACTIVAC STERILE FLUID PATH (SFP) CANISTER ASSY, W/ GEL, 10,ACTIVAC STERILE FLUID PATH (SFP) CANISTER ASSY, W/ GEL 5…
FDA device listing 1454391463 · Sotera Health LLC
Key facts
| Proprietary names | ACTIVAC STERILE FLUID PATH (SFP) CANISTER ASSY, W/ GEL, 10,ACTIVAC STERILE FLUID PATH (SFP) CANISTER ASSY, W/ GEL 5 PK,VAC EXTRA LARGE DRAPE, STAND ALONE, 5 PACK.,VAC GRANUFOAM SILVER MEDIUM DRESSING WITH SENSATRAC - 5 PACK |
|---|---|
| Owner/operator | Sotera Health LLC |
| Owner/operator number | 10029425 |
| Product codes | OMP |
| Device names | OMP - Negative Pressure Wound Therapy Powered Suction Pump |
| Device class | Class II |
| Classification regulations (21 CFR) | 878.4780 |
| Review panels | General & Plastic Surgery |
| Registered establishments | Sterigenics U.S., LLC |
| Establishment registrations | 2022435, 2029275 |
| FEI numbers | 2022435, 1000306431 |
| Establishment operations | Contract Sterilizer |
| 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