FDA device listing
Lifemotion Cart, LMF-10-001,Standalone Oxygenator Holder, LMF-13-001
FDA device listing 1635806464 · Lifemotion Medical Technology Co., Ltd.
Key facts
| Proprietary names | Lifemotion Cart, LMF-10-001,Standalone Oxygenator Holder, LMF-13-001 |
|---|---|
| Owner/operator | Lifemotion Medical Technology Co., Ltd. |
| Owner/operator number | 10083864 |
| Product codes | KRI |
| Device names | KRI - Accessory Equipment, Cardiopulmonary Bypass |
| Device class | Class I |
| Classification regulations (21 CFR) | 870.4200 |
| Review panels | Cardiovascular |
| Registered establishments | LIFEMOTION MEDICAL LIMITED., LIFEMOTION MEDICAL TECHNOLOGY CO., LTD. |
| Establishment registrations | 3021599320, 3045892899 |
| FEI numbers | 3021599320, 3045892899 |
| Establishment operations | Contract Manufacturer, Foreign Exporter, 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