FDA device listing
DHF 0.2 Hemoconcentrator (DHF 02); DHF 0.6 Hemoconcentrator (DHF 06); SH 14 Hemoconcentrator (SH 14)
FDA device listing 2040116090 · Mozarc Medical US LLC
Key facts
| Proprietary names | DHF 0.2 Hemoconcentrator (DHF 02); DHF 0.6 Hemoconcentrator (DHF 06); SH 14 Hemoconcentrator (SH 14) |
|---|---|
| Owner/operator | Mozarc Medical US LLC |
| Owner/operator number | 10090982 |
| Product codes | KDI |
| Device names | KDI - Dialyzer, High Permeability With Or Without Sealed Dialysate System |
| Device class | Class II |
| Classification regulations (21 CFR) | 876.5860 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | BELLCO Srl |
| Establishment registrations | 1000312731 |
| FEI numbers | 1000312731 |
| Establishment operations | Contract Manufacturer |
| 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