Grand Design Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Grand Design Sdn. Bhd. makes
Grand Design Sdn. Bhd. manufactures latex patient examination gloves, designed for single-use medical procedures requiring barrier protection.
These gloves 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 K892608
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Grand Design Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Grand Design Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Grand Design Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Grand Design Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Grand Design Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Grand Design Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Grand Design Sdn. Bhd. in the registry?
The most recently registered devices listed for Grand Design Sdn. Bhd. include PATIENT EXAMINATION GLOVES (LATEX).