FDA device listing
STERRAD 100 NX EXPRESS Test Pack (20123)
FDA device listing 1481383697 · Advanced Sterilization Products
Key facts
| Proprietary names | STERRAD 100 NX EXPRESS Test Pack (20123) |
|---|---|
| Owner/operator | Advanced Sterilization Products |
| Owner/operator number | 9068155 |
| Premarket submissions | K092755 |
| Product codes | FRC |
| Device names | FRC - Indicator, Biological Sterilization Process |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.2800 |
| Review panels | General Hospital |
| Registered establishments | ADVANCED STERILIZATION PRODUCTS |
| Establishment registrations | 2084725 |
| FEI numbers | 3003662624 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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