Golden Charter, Ltd.
Hong Kong SAR ChinaFDA applicant, unverified
- Devices
- 1
What Golden Charter, Ltd. makes
Golden Charter, Ltd. manufactures MEDI and CURI examination gloves, which are designed for single-use medical procedures to provide barrier protection for healthcare professionals.
These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Medi, Curi Exam Gloves Ref K893060
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Golden Charter, Ltd. have in the registry?
The registry currently lists 1 device for Golden Charter, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Golden Charter, Ltd.'s devices?
Among its 1 most recently registered device, Golden Charter, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Golden Charter, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Golden Charter, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Golden Charter, Ltd. in the registry?
The most recently registered devices listed for Golden Charter, Ltd. include MEDI, CURI EXAM GLOVES.