Bluemtech
Country not established
- Devices
- 1
What Bluemtech makes
Bluemtech manufactures solid gel pads designed for medical applications, including wound care and pressure injury prevention. These products are intended to provide cushioning and moisture management in clinical settings, such as hospital beds and medical devices.
The company’s portfolio is regulated under Class II medical devices in the United States, with products authorised through the FDA’s 510(k) clearance process. These devices are listed in the FDA’s 510(k) registry.
Catalogue
Solid Gel Pad Ref K131905
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bluemtech have in the registry?
The registry currently lists 1 device for Bluemtech. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bluemtech's devices?
Among its 1 most recently registered device, Bluemtech has devices listed in FDA 510(k) (1 device).
What risk classes do Bluemtech's devices fall under?
Among its 1 most recently registered device, the classes recorded for Bluemtech's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bluemtech in the registry?
The most recently registered devices listed for Bluemtech include SOLID GEL PAD.