Medtronic Blood Management
Country not established
- Devices
- 3
What Medtronic Blood Management makes
Medtronic Blood Management produces electronic quality control systems for blood products, such as the HEPTRAC, and autotransfusion apparatus designed to collect and reinfuse a patient’s own blood during surgery. These devices support intraoperative blood salvage and ensure the integrity of blood components through automated testing and processing.
The company’s portfolio is regulated under FDA’s Class II device classification, with products authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) database, reflecting their compliance with US regulatory requirements. The manufacturer operates from the United States.
Catalogue
Heptrac Electronic Quality Control Ref K981815
Regimes: 510(k) Registry: 510(k)Autotransfusion Appartus (Autolog) Ref K972894
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic Blood Management have in the registry?
The registry currently lists 3 devices for Medtronic Blood Management. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic Blood Management's devices?
Among its 3 most recently registered devices, Medtronic Blood Management has devices listed in FDA 510(k) (3 devices).
What risk classes do Medtronic Blood Management's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Medtronic Blood Management's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic Blood Management in the registry?
The most recently registered devices listed for Medtronic Blood Management include HEPTRAC ELECTRONIC QUALITY CONTROL, AUTOTRANSFUSION APPARTUS (AUTOLOG) and MODIFICATION OF AUTOTRANSFUSION APPARATUS (AUTOLOG).