Med-West, Inc.
United StatesFDA applicant, unverified
- Devices
- 11
What Med-West, Inc. makes
Med-West, Inc. manufactures single-needle subclavian vein access devices, including the MWI250/260 and MWI 888/666 double-lumen variants, as well as subclavian vein catheters for medical procedures. Their portfolio includes contrast injection devices, Teflon-coated femoral catheters (MWI 100, 10), and injection caps (MNI 400). They also produce acute hemodialysis trays, cardioplegia-air aspiration devices (CPC), wound dressings (MWI 400), sheath/dilators, and a power toilet elevator.
The company’s devices are classified under FDA regulations as Class I or Class II, with submissions recorded in the FDA’s 510(k) clearance registry. Products are listed under U.S. jurisdiction, adhering to domestic medical device compliance standards.
Catalogue
Search and filter all 11 devicesFrequently asked questions
How many devices does Med-West, Inc. have in the registry?
The registry currently lists 11 devices for Med-West, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Med-West, Inc.'s devices?
Among its 11 most recently registered devices, Med-West, Inc. has devices listed in FDA 510(k) (11 devices).
What risk classes do Med-West, Inc.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for Med-West, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Med-West, Inc. in the registry?
The most recently registered devices listed for Med-West, Inc. include SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260, CONTRAST INJECTION DEVICE, TEFLON FEMORAL CATHETER MWI 100, 10 & and MNI 400 INJECTION CAPS.