Mulpha Intl. Trading Corp. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 6
What Mulpha Intl. Trading Corp. Bhd. makes
Mulpha Intl. Trading Corp. Bhd. manufactures patient examination gloves sourced from multiple manufacturers, including Getah Gayal, AEK Rubber Products, Healthcare Gloves, M.R. Rubber Industries, Palmbase Rubber MFG., and Terang Nusa.
These products are classified as Class I medical devices and are listed under the FDA’s 510(k) registry. The company operates from the United States.
Catalogue
Patient Exam Gloves (Mfg. Getah Gayal) Ref K891812
Regimes: 510(k) Registry: 510(k)Patient Exam Gloves (Mfg. Aek Rubber Products) Ref K891813
Regimes: 510(k) Registry: 510(k)Patient Exam Gloves (Mfg. Healthcare Gloves) Ref K891816
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Patient Exam Gloves (Mfg. Palmbase Rubber Mfg.) Ref K891811
Regimes: 510(k) Registry: 510(k)Patient Exam Gloves (Mfg. Terang Nusa) Ref K891817
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mulpha Intl. Trading Corp. Bhd. have in the registry?
The registry currently lists 6 devices for Mulpha Intl. Trading Corp. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mulpha Intl. Trading Corp. Bhd.'s devices?
Among its 6 most recently registered devices, Mulpha Intl. Trading Corp. Bhd. has devices listed in FDA 510(k) (6 devices).
What risk classes do Mulpha Intl. Trading Corp. Bhd.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Mulpha Intl. Trading Corp. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Mulpha Intl. Trading Corp. Bhd. in the registry?
The most recently registered devices listed for Mulpha Intl. Trading Corp. Bhd. include PATIENT EXAM GLOVES (MFG. GETAH GAYAL), PATIENT EXAM GLOVES (MFG. AEK RUBBER PRODUCTS), PATIENT EXAM GLOVES (MFG. HEALTHCARE GLOVES) and PATIENT EXAM GLOVES (MFG. M.R. RUBBER INDUSTRIES).