Wesco International, Inc.
Country not established
- Devices
- 5
What Wesco International, Inc. makes
Wesco International, Inc. manufactures nitrile examination and treatment gloves that are non-powdered and non-antimicrobial, designed for medical and clinical use. The product line includes multiple variants of the Actuvate glove, which are intended for protective barrier applications during patient care procedures.
The company’s portfolio is classified under FDA’s Class I medical devices and is listed in the FDA’s Unique Device Identification (UDI) system. The manufacturer operates from the United States, adhering to applicable regulatory requirements for these device categories.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- DUNS number
- 884051616
Frequently asked questions
How many devices does Wesco International, Inc. have in the registry?
The registry currently lists 5 devices for Wesco International, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wesco International, Inc.'s devices?
Among its 5 most recently registered devices, Wesco International, Inc. has devices listed in FDA GUDID (5 devices).
What risk classes do Wesco International, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Wesco International, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Wesco International, Inc. in the registry?
The most recently registered devices listed for Wesco International, Inc. include Actuvate ACTU75526, Actuvate ACTU75530, Actuvate ACTU75525 and Actuvate ACTU75528.