FDA device listing
Adaptive Nomogram Transfer Pack,Fenwal Plasmalink Transfer Pack Container with Luer Adapter and No Outlet Ports
FDA device listing 1070754333 · Fresenius Kabi AG
Key facts
| Proprietary names | Adaptive Nomogram Transfer Pack,Fenwal Plasmalink Transfer Pack Container with Luer Adapter and No Outlet Ports |
|---|---|
| Owner/operator | Fresenius Kabi AG |
| Owner/operator number | 9027285 |
| Premarket submissions | BK190421 |
| Product codes | KSR |
| Device names | KSR - Container, Empty, For Collection & Processing Of Blood & Blood Components |
| Device class | Class II |
| Classification regulations (21 CFR) | 864.9100 |
| Review panels | Hematology |
| Registered establishments | FENWAL, INC., FENWAL INTERNATIONAL, INC. |
| Establishment registrations | 9612051, 3004548776 |
| FEI numbers | 3002806457, 3004548776 |
| Establishment operations | Complaint File Establishment, Specification Developer, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None 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