Rubberex (M) Sdn Berhad
MalaysiaFDA applicant, unverified
- Devices
- 2
What Rubberex (M) Sdn Berhad makes
Rubberex (M) Sdn Berhad manufactures patient examination gloves, including latex-free versions with corn starch powder and standard latex gloves. These products are designed for single-use medical and clinical examinations to maintain hygiene and reduce contamination risk.
The company’s portfolio is classified under Class I medical devices and is listed in the FDA’s 510(k) registry. The manufacturer is based in the US.
Catalogue
Patient Examination Gloves W/Corn Starch Powder Ref K893782
Regimes: 510(k) Registry: 510(k)Patient Examination Gloves (Latex) Ref K891389
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rubberex (M) Sdn Berhad have in the registry?
The registry currently lists 2 devices for Rubberex (M) Sdn Berhad. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rubberex (M) Sdn Berhad's devices?
Among its 2 most recently registered devices, Rubberex (M) Sdn Berhad has devices listed in FDA 510(k) (2 devices).
What risk classes do Rubberex (M) Sdn Berhad's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Rubberex (M) Sdn Berhad's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Rubberex (M) Sdn Berhad in the registry?
The most recently registered devices listed for Rubberex (M) Sdn Berhad include PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER and PATIENT EXAMINATION GLOVES (LATEX).