FDA device listing
Jiangsu
FDA device listing 1300636629 · HOSPICIO LA PAZ
Key facts
| Proprietary names | Jiangsu |
|---|---|
| Owner/operator | HOSPICIO LA PAZ |
| Owner/operator number | 10048811 |
| Product codes | LDE |
| Device names | LDE - Stethoscope, Manual |
| Device class | Class I |
| Classification regulations (21 CFR) | 870.1875 |
| Review panels | Cardiovascular |
| Registered establishments | HOSPICIO LAPAZ INC |
| Establishment registrations | 3011489684 |
| FEI numbers | 3011489684 |
| Establishment operations | Complaint File Establishment |
| 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