Mediaid Inc
United StatesFDA applicant, unverified
Mediaid Inc is a medical device manufacturer, with 210 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 14 Nov 2026.
- Devices
- 210
Registry facts
- Registries
- FDA GUDID 206
- FDA 510(k) 4
- Device classes
- FDA Class II 210
- Identifiers
- DUNS 134990550
What Mediaid Inc makes
MediaID Inc manufactures pulse oximeter sensors designed for continuous oxygen saturation (SpO2) monitoring, including adhesive disposable sensors with foam or medical-grade tape for pediatric, neonatal, and infant use, as well as reusable soft sensors for adult and pediatric patients.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance and the FDA’s Unique Device Identifier (UDI) system. The company operates from the United States.
Catalogue
Search and filter all 210 devicesShowing 1-50 of 210
Company details
- DUNS number
- 134990550
Frequently asked questions
How many devices does MEDIAID INC have in the registry?
The registry currently lists 210 devices for MEDIAID INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list MEDIAID INC's devices?
Among its 50 most recently registered devices, MEDIAID INC has devices listed in FDA GUDID (50 devices).
What risk classes do MEDIAID INC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for MEDIAID INC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from MEDIAID INC in the registry?
The most recently registered devices listed for MEDIAID INC include Adhesive Disposable SpO2 Sensors with Micro Foam Tape - Pediatric CST020-2902, Adhesive Disposable SpO2 Sensors with Medaplast Tape - Pediatric CST034-2702, Adhesive Disposable Sensors with Transpore Tape - Pediatric CST032-2962 and Reusable Sensor - Soft Adult CST100-3126.