Mediglove Sdn. Bhd.
Country not established
- Devices
- 2
What Mediglove Sdn. Bhd. makes
Mediglove Sdn. Bhd. manufactures latex patient examination gloves designed for clinical use, including single-use and reusable variants for medical examinations.
These products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K892011
Regimes: 510(k) Registry: 510(k)Patient Examination Glove (Latex) Ref K892008
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mediglove Sdn. Bhd. have in the registry?
The registry currently lists 2 devices for Mediglove Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mediglove Sdn. Bhd.'s devices?
Among its 2 most recently registered devices, Mediglove Sdn. Bhd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Mediglove Sdn. Bhd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Mediglove Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Mediglove Sdn. Bhd. in the registry?
The most recently registered devices listed for Mediglove Sdn. Bhd. include PATIENT EXAMINATION GLOVES (LATEX) and PATIENT EXAMINATION GLOVE (LATEX).