FDA device listing
Half Day INFUSOR 5 ml/h Portable Elastomeric Infusion System,INFUSOR 5 ML/H,MULTI-DAY INFUSOR,Multiday INFUSOR 0.5 ml/h…
FDA device listing 1237176220 · Sotera Health LLC
Key facts
| Proprietary names | Half Day INFUSOR 5 ml/h Portable Elastomeric Infusion System,INFUSOR 5 ML/H,MULTI-DAY INFUSOR,Multiday INFUSOR 0.5 ml/h Portable Elastomeric Infusion System,SEVENDAY INFUSOR, O.5ML/HR,SINGLE DAY INFUSOR,Singleday INFUSOR 2ml Portable Elastomeric Infusion System,TWO DAY INFUSOR 2 ML/H,Two Day INFUSOR 2 ml/h Portable Elastomeric Infusion System |
|---|---|
| Owner/operator | Sotera Health LLC |
| Owner/operator number | 10029425 |
| Product codes | MEB |
| Device names | MEB - Pump, Infusion, Elastomeric |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.5725 |
| Review panels | General Hospital |
| Registered establishments | Sterigenics U.S., LLC |
| Establishment registrations | 2029275 |
| FEI numbers | 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