Repro-Med Systems, Inc. Dba Rms Medical Products
United StatesFDA applicant, unverified
- Devices
- 3
What Repro-Med Systems, Inc. Dba Rms Medical Products makes
Repro-Med Systems, Inc. manufactures subcutaneous needle sets, including the High-Flo Super26 series, and an infusion system called the Integrated Catch-up Freedom Syringe Driver. These products are designed for controlled subcutaneous administration of fluids or medications.
The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The portfolio is regulated in the United States, where the manufacturer is based.
Catalogue
- Regimes: 510(k) Registry: 510(k)
HIgH-Flo Super26 Subcutaneous Needle Sets Ref K180843
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Repro-Med Systems, Inc. Dba Rms Medical Products have in the registry?
The registry currently lists 3 devices for Repro-Med Systems, Inc. Dba Rms Medical Products. Devices recorded under merged duplicate company entries are counted once.
Which registries list Repro-Med Systems, Inc. Dba Rms Medical Products's devices?
Among its 3 most recently registered devices, Repro-Med Systems, Inc. Dba Rms Medical Products has devices listed in FDA 510(k) (3 devices).
What risk classes do Repro-Med Systems, Inc. Dba Rms Medical Products's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Repro-Med Systems, Inc. Dba Rms Medical Products's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Repro-Med Systems, Inc. Dba Rms Medical Products in the registry?
The most recently registered devices listed for Repro-Med Systems, Inc. Dba Rms Medical Products include MODEL NUMBER: RMS1-2604, RMS1-2614, RMS1-2404, RMS1-2414, RMS2-2604, RMS2-2614, RMS2-2404, RMS2-2414, RMS3-2604, RMS3-26, HIgH-Flo Super26 Subcutaneous Needle Sets and Integrated Catch-up Freedom Syringe Driver Infusion System.