FDA device listing
Inflation Device
FDA device listing 1210863879 · Lepu Medical Technology (Beijing) Co., Ltd
Key facts
| Proprietary names | Inflation Device |
|---|---|
| Owner/operator | Lepu Medical Technology (Beijing) Co., Ltd |
| Owner/operator number | 10038811 |
| Product codes | PTM |
| Device names | PTM - Syringe, Balloon Inflation, Exempt |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.1650 |
| Review panels | Cardiovascular |
| Registered establishments | Beijing Target Medical Technologies Inc., LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD |
| Establishment registrations | 3008002401, 3011564431, 3018312328 |
| FEI numbers | 3008002401, 3011564431, 3018312328 |
| Establishment operations | Contract Sterilizer, 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