Chien Lung Rubber Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 1
What Chien Lung Rubber Co., Ltd. makes
Chien Lung Rubber Co., Ltd. manufactures patient examination gloves made of latex, intended for single‑use clinical use.
These gloves are classified as Class I medical devices and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K892744
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Chien Lung Rubber Co., Ltd. have in the registry?
The registry currently lists 1 device for Chien Lung Rubber Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Chien Lung Rubber Co., Ltd.'s devices?
Among its 1 most recently registered device, Chien Lung Rubber Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Chien Lung Rubber Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Chien Lung Rubber Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Chien Lung Rubber Co., Ltd. in the registry?
The most recently registered devices listed for Chien Lung Rubber Co., Ltd. include PATIENT EXAMINATION GLOVES (LATEX).