Wedana Rubber Products
MalaysiaFDA applicant, unverified
- Devices
- 1
What Wedana Rubber Products makes
Wedana Rubber Products manufactures patient examination gloves, designed for single-use medical procedures to ensure hygiene and barrier protection during clinical examinations.
The company’s portfolio is regulated under FDA’s Class I device classification, with products listed via the 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Patient Examination Gloves Ref K893607
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wedana Rubber Products have in the registry?
The registry currently lists 1 device for Wedana Rubber Products. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wedana Rubber Products's devices?
Among its 1 most recently registered device, Wedana Rubber Products has devices listed in FDA 510(k) (1 device).
What risk classes do Wedana Rubber Products's devices fall under?
Among its 1 most recently registered device, the classes recorded for Wedana Rubber Products's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Wedana Rubber Products in the registry?
The most recently registered devices listed for Wedana Rubber Products include PATIENT EXAMINATION GLOVES.