Dipform Rubber Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Dipform Rubber Sdn. Bhd. makes
Dipform Rubber Sdn. Bhd. manufactures latex patient examination gloves, designed for single-use medical procedures and examinations.
These gloves are classified as Class I devices under regulatory frameworks and are listed via the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examination Glove (Latex) Ref K892014
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dipform Rubber Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Dipform Rubber Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dipform Rubber Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Dipform Rubber Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Dipform Rubber Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dipform Rubber Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dipform Rubber Sdn. Bhd. in the registry?
The most recently registered devices listed for Dipform Rubber Sdn. Bhd. include PATIENT EXAMINATION GLOVE (LATEX).