Ineedmd
Country not established
- Devices
- 2
What Ineedmd makes
The company produces single-use 12-lead ECG gloves designed for electrocardiogram procedures, facilitating electrode attachment and signal transmission during cardiac monitoring.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
12 Lead Glove Ref K100315
Regimes: 510(k) Registry: 510(k)12-Lead Glove Ref K033559
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ineedmd have in the registry?
The registry currently lists 2 devices for Ineedmd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ineedmd's devices?
Among its 2 most recently registered devices, Ineedmd has devices listed in FDA 510(k) (2 devices).
What risk classes do Ineedmd's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ineedmd's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ineedmd in the registry?
The most recently registered devices listed for Ineedmd include 12 LEAD GLOVE and 12-LEAD GLOVE.