Dubo Latex, Ltd.
Country not established
- Devices
- 1
What Dubo Latex, Ltd. makes
Dubo Latex, Ltd. manufactures patient examination gloves, which are single-use barrier devices designed for medical and clinical examinations to prevent cross-contamination.
The company’s products fall under FDA Class I medical devices and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Patient Examination Gloves Ref K892974
510(k) 510(k)
Frequently asked questions
How many devices does Dubo Latex, Ltd. have in the registry?
The registry currently lists 1 device for Dubo Latex, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dubo Latex, Ltd.'s devices?
Among its 1 most recently registered device, Dubo Latex, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Dubo Latex, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dubo Latex, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dubo Latex, Ltd. in the registry?
The most recently registered devices listed for Dubo Latex, Ltd. include PATIENT EXAMINATION GLOVES.