FDA device listing
INTERCEPT Blood System for Platelets
FDA device listing 1713799253 · Cerus Corporation
Key facts
| Proprietary names | INTERCEPT Blood System for Platelets |
|---|---|
| Owner/operator | Cerus Corporation |
| Owner/operator number | 10048354 |
| Premarket submissions | BP140143 |
| Product codes | PJF |
| Device names | PJF - Illuminator System For Blood Products |
| Device class | Class III |
| Classification regulations (21 CFR) | ORCA1.PJF |
| Review panels | Hematology |
| Registered establishments | CERUS CORPORATION, Cerus Europe BV |
| Establishment registrations | 3003925919, 3007170494 |
| FEI numbers | 3003925919, 3007170494 |
| Establishment operations | Complaint File Establishment, Specification Developer, Foreign Exporter, Repackager/Relabeler |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 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