Medical Device Manufacturer · DE , Helmbrechts

Raumedic AG

6 submissions · 6 cleared · Since 2011
6
Total
6
Cleared
0
Denied

Raumedic AG has 6 FDA 510(k) cleared medical devices. Based in Helmbrechts, DE.

Latest FDA clearance: Aug 2025. Active since 2011. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Raumedic AG Filter by specialty or product code using the sidebar.

6 devices
1–6 of 6
NEUROVENT-P (092946-003); NEUROVENT (092956-003); NEUROVENT-IFD-R (095317-003); NEUROVENT-IFD-S (091678-003); NEUROVENT-P-TEMP (094268-003); NEUROVENT-TEMP (094278-003); NEUROVENT-TEMP-IFD-R (095327-003); NEUROVENT-TEMP-IFD-S (094288-003); NEUROVENT-PTO (095008-003); NEUROVENT-PTO 2L (095108-003); NEUROVENT-PX (091580-003); BOLT-DRILL KIT CH5 (091888-003); BOLT-DRILL KIT CH9 (091898-003); BOLT-DRILL KIT PTO (092380-003); BOLT-DRILL KIT VP 16 (092969-003); BOLT KIT CH5 (091868-003); BOL
K250285 · GWM Device, Monitoring, Intracranial Pressure · Neurology
Aug 2025 210d
MPR2 logO DATALOGGER
K171666 · GWM Device, Monitoring, Intracranial Pressure · Neurology
Jul 2017 31d
RAUMEDIC-PTO-MONITORING-SYSTEM
K130529 · GWM Device, Monitoring, Intracranial Pressure · Neurology
Oct 2013 238d
RAUMEDIC-ICP-TEMP-MONITORING-SYSTEM
K120252 · GWM Device, Monitoring, Intracranial Pressure · Neurology
Apr 2012 75d
RAUMEDIC ICP MONITORING SYSTEM
K112017 · GWM Device, Monitoring, Intracranial Pressure · Neurology
Oct 2011 89d
RAUMEDIC- ICP-MONITORING SYSTEM
K103206 · GWM Device, Monitoring, Intracranial Pressure · Neurology
Mar 2011 123d
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