Hwa Shun Rubber Ent. Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 1
What Hwa Shun Rubber Ent. Co., Ltd. makes
The company manufactures latex patient examination gloves, designed for single-use medical procedures to maintain hygiene and reduce infection risk during clinical examinations.
These gloves 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
Patient Examination Gloves (Latex) Ref K892468
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hwa Shun Rubber Ent. Co., Ltd. have in the registry?
The registry currently lists 1 device for Hwa Shun Rubber Ent. Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hwa Shun Rubber Ent. Co., Ltd.'s devices?
Among its 1 most recently registered device, Hwa Shun Rubber Ent. Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Hwa Shun Rubber Ent. Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hwa Shun Rubber Ent. Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Hwa Shun Rubber Ent. Co., Ltd. in the registry?
The most recently registered devices listed for Hwa Shun Rubber Ent. Co., Ltd. include PATIENT EXAMINATION GLOVES (LATEX).