Direct Marketing USA LLC
Country not established
- Devices
- 20
What Direct Marketing USA LLC makes
Direct Marketing USA LLC manufactures nitrile examination and treatment gloves that are non-powdered and non-antimicrobial. These products are designed for medical and clinical use, ensuring barrier protection during procedures.
The company’s portfolio consists of Class I medical devices, all of which are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates within the United States.
Catalogue
Search and filter all 20 devicesCompany details
- DUNS number
- 079327950
Frequently asked questions
How many devices does Direct Marketing USA LLC have in the registry?
The registry currently lists 20 devices for Direct Marketing USA LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Direct Marketing USA LLC's devices?
Among its 20 most recently registered devices, Direct Marketing USA LLC has devices listed in FDA GUDID (20 devices).
What risk classes do Direct Marketing USA LLC's devices fall under?
Among its 20 most recently registered devices, the classes recorded for Direct Marketing USA LLC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Direct Marketing USA LLC in the registry?
The most recently registered devices listed for Direct Marketing USA LLC include Finesse DGN502, Nu Flex 4504003, Vintage VGN3E and Nu Flex 4504002.