Butex Products (M'Sia) Sdn.Bhd
MalaysiaFDA 510(k) applicant, unverified
- Devices
- 1
What Butex Products (M'Sia) Sdn.Bhd makes
Butex Products (M'Sia) Sdn.Bhd manufactures natural latex patient examination gloves, designed for clinical use during medical procedures and examinations.
These gloves are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway in the United States.
Catalogue
Patient Examination Gloves (Natural Latex) Ref K891967
510(k) 510(k)
Frequently asked questions
How many devices does Butex Products (M'Sia) Sdn.Bhd have in the registry?
The registry currently lists 1 device for Butex Products (M'Sia) Sdn.Bhd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Butex Products (M'Sia) Sdn.Bhd's devices?
Among its 1 most recently registered device, Butex Products (M'Sia) Sdn.Bhd has devices listed in FDA 510(k) (1 device).
What risk classes do Butex Products (M'Sia) Sdn.Bhd's devices fall under?
Among its 1 most recently registered device, the classes recorded for Butex Products (M'Sia) Sdn.Bhd's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Butex Products (M'Sia) Sdn.Bhd in the registry?
The most recently registered devices listed for Butex Products (M'Sia) Sdn.Bhd include PATIENT EXAMINATION GLOVES (NATURAL LATEX).