Medireach, Inc.
Country not established
- Devices
- 1
What Medireach, Inc. makes
Medireach, Inc. manufactures external urinary drainage catheters designed for female patients, including the PRIMROSE Female External Catheter.
These devices are regulated as Class II under the FDA and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medireach, Inc. have in the registry?
The registry currently lists 1 device for Medireach, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medireach, Inc.'s devices?
Among its 1 most recently registered device, Medireach, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medireach, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medireach, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medireach, Inc. in the registry?
The most recently registered devices listed for Medireach, Inc. include PRIMROSE FEMALE EXT. CATH OR EXT. URINARY DRAINAGE.