Wei Ming Industry Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Patient Examination Gloves (Latex) Ref K891429
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wei Ming Industry Co., Ltd. have in the registry?
The registry currently lists 1 device for Wei Ming Industry Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wei Ming Industry Co., Ltd.'s devices?
Among its 1 most recently registered device, Wei Ming Industry Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Wei Ming Industry Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Wei Ming Industry Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Wei Ming Industry Co., Ltd. in the registry?
The most recently registered devices listed for Wei Ming Industry Co., Ltd. include PATIENT EXAMINATION GLOVES (LATEX).