Madafair, Ltd.
Hong Kong SAR ChinaFDA applicant, unverified
- Devices
- 1
What Madafair, Ltd. makes
Madafair, Ltd. manufactures latex patient examination gloves, designed for single-use medical procedures to maintain hygiene and reduce infection risk during clinical examinations.
These gloves are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K892095
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Madafair, Ltd. have in the registry?
The registry currently lists 1 device for Madafair, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Madafair, Ltd.'s devices?
Among its 1 most recently registered device, Madafair, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Madafair, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Madafair, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Madafair, Ltd. in the registry?
The most recently registered devices listed for Madafair, Ltd. include PATIENT EXAMINATION GLOVES (LATEX).