Mia Secret
Country not established
- Devices
- 4
What Mia Secret makes
The company produces nitrile examination and treatment gloves that are non-powdered and non-antimicrobial, designed for medical and procedural use.
These devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- DUNS number
- 118924410
Frequently asked questions
How many devices does MIA SECRET have in the registry?
The registry currently lists 4 devices for MIA SECRET. Devices recorded under merged duplicate company entries are counted once.
Which registries list MIA SECRET's devices?
Among its 4 most recently registered devices, MIA SECRET has devices listed in FDA GUDID (4 devices).
What risk classes do MIA SECRET's devices fall under?
Among its 4 most recently registered devices, the classes recorded for MIA SECRET's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from MIA SECRET in the registry?
The most recently registered devices listed for MIA SECRET include Mia Secret NGL-1215, Mia Secret NGS-1205, Mia Secret NGXL-1220 and Mia Secret NGM-1210.