Pelangi Rubber Products Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Pelangi Rubber Products Sdn. Bhd. makes
Pelangi Rubber Products Sdn. Bhd. makes patient exam gloves under the brand names QUEST and PELANGI, specifically latex gloves intended for medical examination use.
These devices are classified as Class I medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
'quest', 'pelangi' Patient Exam Gloves (Latex) Ref K891272
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pelangi Rubber Products Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Pelangi Rubber Products Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pelangi Rubber Products Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Pelangi Rubber Products Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Pelangi Rubber Products Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pelangi Rubber Products Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Pelangi Rubber Products Sdn. Bhd. in the registry?
The most recently registered devices listed for Pelangi Rubber Products Sdn. Bhd. include 'QUEST', 'PELANGI' PATIENT EXAM GLOVES (LATEX).