Midwest Reprocessing Center, LLC
United StatesFDA applicant, unverified
- Devices
- 4
What Midwest Reprocessing Center, LLC makes
Midwest Reprocessing Center, LLC reprocesses single-use medical devices, including venodyne sleeves and foot cuffs, pulse oximeter probes, LNCS and Oximax sensors, and SCD Express and ALP sleeves/foot cuffs for reuse in clinical settings.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records in the FDA registry. The company operates within the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Midwest Reprocessing Center, LLC have in the registry?
The registry currently lists 4 devices for Midwest Reprocessing Center, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Midwest Reprocessing Center, LLC's devices?
Among its 4 most recently registered devices, Midwest Reprocessing Center, LLC has devices listed in FDA 510(k) (4 devices).
What risk classes do Midwest Reprocessing Center, LLC's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Midwest Reprocessing Center, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Midwest Reprocessing Center, LLC in the registry?
The most recently registered devices listed for Midwest Reprocessing Center, LLC include MIDWEST REPROCESSING CENTER REPROCESSED VENODYNE SLEEVES/FOOT CUFFS, MIDWESTERN REPROCESSING CENTER REPROCESSED PULSE OXIMETER PROBE, MIDWEST REPROCESSING CENTER REPROCESSED LNCS SESSORS; MIDWEST REPROCESSING CENTER REPROCESSED OXIMAX SENSORS; MIDWEST RE and MIDWEST REPROCESSING CENTER REPROCESSED SCD EXPRESS SLEEVES/ FOOT CUFFS, MIDWEST REPROCESSING CENTER REPROCESSED ALP SLE.