Imed Corp.
United StatesFDA applicant, unverified
- Devices
- 43
What Imed Corp. makes
Imed Corp. manufactures volumetric infusion pumps, administration sets, and intravenous filtration systems for controlled drug delivery and fluid administration. Products include ambulatory pumps, Y-type connectors for blood/solution infusion, vented/non-vented administration sets with safety valves, and cassette-based infusion systems. The portfolio also covers intravenous sets for gravity-fed infusions and modified infusion pumps for specialized use.
The company’s devices are regulated under FDA 510(k) clearance, with products classified as Class I and Class II medical devices. These products are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Search and filter all 43 devicesFrequently asked questions
How many devices does Imed Corp. have in the registry?
The registry currently lists 43 devices for Imed Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Imed Corp.'s devices?
Among its 43 most recently registered devices, Imed Corp. has devices listed in FDA 510(k) (43 devices).
What risk classes do Imed Corp.'s devices fall under?
Among its 43 most recently registered devices, the classes recorded for Imed Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Imed Corp. in the registry?
The most recently registered devices listed for Imed Corp. include THE IMED AMBULATORY INFUSION PUMP, ADMINISTRATION SETS, MACRODOT ADD-I-MED ADMIN. SET, IMED GEMINI 12 NONVENTED Y-TYPE BLOOD/SOLUTION ADM and IMED(R) GEMINI(TM) PC-1 VOLUMETRIC INFUSION PUMP.