Pai Hoi Ent., Ltd.
Country not established
- Devices
- 1
What Pai Hoi Ent., Ltd. makes
Pai Hoi Ent., Ltd. manufactures latex patient examination gloves designed for medical use, providing a barrier for healthcare professionals during clinical examinations.
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 K891831
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pai Hoi Ent., Ltd. have in the registry?
The registry currently lists 1 device for Pai Hoi Ent., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pai Hoi Ent., Ltd.'s devices?
Among its 1 most recently registered device, Pai Hoi Ent., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Pai Hoi Ent., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pai Hoi Ent., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Pai Hoi Ent., Ltd. in the registry?
The most recently registered devices listed for Pai Hoi Ent., Ltd. include PATIENT EXAMINATION GLOVES (LATEX).