Medi Pure Corp.
MadagascarFDA applicant, unverified
- Devices
- 1
What Medi Pure Corp. makes
Medi Pure Corp. manufactures latex patient examination gloves designed for clinical use, providing a barrier for healthcare professionals during medical procedures.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Latex Patient Examination Gloves Ref K924356
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medi Pure Corp. have in the registry?
The registry currently lists 1 device for Medi Pure Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medi Pure Corp.'s devices?
Among its 1 most recently registered device, Medi Pure Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Medi Pure Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medi Pure Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Medi Pure Corp. in the registry?
The most recently registered devices listed for Medi Pure Corp. include LATEX PATIENT EXAMINATION GLOVES.