FDA device listing
Automated External Defibrillators (Non-Wearable)
FDA device listing 1736983868 · LEONHARD LANG GMBH
Key facts
| Owner/operator | LEONHARD LANG GMBH |
|---|---|
| Owner/operator number | 8020045 |
| Product codes | MKJ, MLN |
| Device names | MKJ - Automated External Defibrillators (Non-Wearable), MLN - Electrode, Electrocardiograph, Multi-Function |
| Device class | Class II, Class III |
| Classification regulations (21 CFR) | 870.2360, 870.5310 |
| Review panels | Cardiovascular |
| Registered establishments | LEONHARD LANG GMBH |
| Establishment registrations | 8020045 |
| FEI numbers | 6736 |
| 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