FDA device listing
ADE M118000,ADE M118000-01,ADE M118600,ADE M118600-01,ADE M118600-02,ADE MZ10023-1,ADE MZ10023-2,ADE MZ10023-3,ADE…
FDA device listing 1880000439 · ADE Germany GmbH
Key facts
| Proprietary names | ADE M118000,ADE M118000-01,ADE M118600,ADE M118600-01,ADE M118600-02,ADE MZ10023-1,ADE MZ10023-2,ADE MZ10023-3,ADE MZ10027-1,ADE MZ10028-1,ADE MZ10040,ADE MZ10042 |
|---|---|
| Owner/operator | ADE Germany GmbH |
| Owner/operator number | 10095728 |
| Product codes | FRW |
| Device names | FRW - Scale, Patient |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.2720 |
| Review panels | General Hospital |
| Registered establishments | ADE GERMANY GMBH |
| Establishment registrations | 3044853249 |
| FEI numbers | 3044853249 |
| Establishment operations | 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