Cheng Chang Development Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 1
What Cheng Chang Development Co., Ltd. makes
Cheng Chang Development Co., Ltd. manufactures patient examination gloves, which are designed for single-use medical procedures to maintain hygiene and reduce infection risk during clinical examinations.
These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Patient Examination Gloves Ref K891957
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cheng Chang Development Co., Ltd. have in the registry?
The registry currently lists 1 device for Cheng Chang Development Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cheng Chang Development Co., Ltd.'s devices?
Among its 1 most recently registered device, Cheng Chang Development Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Cheng Chang Development Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cheng Chang Development Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Cheng Chang Development Co., Ltd. in the registry?
The most recently registered devices listed for Cheng Chang Development Co., Ltd. include PATIENT EXAMINATION GLOVES.