Inteplast Group Corporation
Country not established
- Devices
- 9
What Inteplast Group Corporation makes
The company produces nitrile examination and treatment gloves that are non-powdered and non-antimicrobial, designed for medical use.
These devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- DUNS number
- 786941427
Frequently asked questions
How many devices does Inteplast Group Corporation have in the registry?
The registry currently lists 9 devices for Inteplast Group Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inteplast Group Corporation's devices?
Among its 9 most recently registered devices, Inteplast Group Corporation has devices listed in FDA GUDID (9 devices).
What risk classes do Inteplast Group Corporation's devices fall under?
Among its 9 most recently registered devices, the classes recorded for Inteplast Group Corporation's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Inteplast Group Corporation in the registry?
The most recently registered devices listed for Inteplast Group Corporation include Inteplast NF203, Inteplast NBLK002, Inteplast NBLK004 and Inteplast NF205.