Emergo Europe Consulting BV
NetherlandsFDA applicant, unverified
- Devices
- 2
What Emergo Europe Consulting BV makes
Emergo Europe Consulting BV manufactures the ICP TriageManager, a device designed for intracranial pressure (ICP) monitoring and patient triage in critical care settings. It supports real-time monitoring and decision-making for managing patients with elevated ICP, such as those with traumatic brain injury or hydrocephalus.
The ICP TriageManager is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Ceramill Zolid FX Ref K152383
Regimes: 510(k) Registry: 510(k)Icp Triagemanager Ref K122095
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Emergo Europe Consulting BV have in the registry?
The registry currently lists 2 devices for Emergo Europe Consulting BV. Devices recorded under merged duplicate company entries are counted once.
Which registries list Emergo Europe Consulting BV's devices?
Among its 2 most recently registered devices, Emergo Europe Consulting BV has devices listed in FDA 510(k) (2 devices).
What risk classes do Emergo Europe Consulting BV's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Emergo Europe Consulting BV's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Emergo Europe Consulting BV in the registry?
The most recently registered devices listed for Emergo Europe Consulting BV include Ceramill Zolid FX and ICP TRIAGEMANAGER.