Unitex Rubber Industry Co., Ltd.
ThailandFDA 510(k) applicant, unverified
- Devices
- 1
What Unitex Rubber Industry Co., Ltd. makes
Unitex Rubber Industry Co., Ltd. manufactures latex patient examination gloves, designed for use in clinical settings to reduce the risk of infection during medical procedures.
These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K892240
510(k) 510(k)
Frequently asked questions
How many devices does Unitex Rubber Industry Co., Ltd. have in the registry?
The registry currently lists 1 device for Unitex Rubber Industry Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Unitex Rubber Industry Co., Ltd.'s devices?
Among its 1 most recently registered device, Unitex Rubber Industry Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Unitex Rubber Industry Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Unitex Rubber Industry Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Unitex Rubber Industry Co., Ltd. in the registry?
The most recently registered devices listed for Unitex Rubber Industry Co., Ltd. include PATIENT EXAMINATION GLOVES (LATEX).