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Raumedic AG

Active in EUDAMED

Germanyfrom SRN EUDAMED SRN DE-MF-000006155

Raumedic AG is a medical device manufacturer based in Germany, with 108 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II; EU Class I, IIa and IIb) as of 13 Nov 2026.

Devices
108
Registrations
EUDAMED

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 75
  • EUDAMED 55
  • FDA 510(k) 6

A device listed in two registries counts in both.

Device classes
  • FDA Class II 80
  • EU Class I 25
  • EU Class IIa 2
  • EU Class IIb 1
Top EMDN categories
Identifiers
  • EUDAMED SRN DE-MF-000006155
  • DUNS 332785323

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor

What Raumedic AG makes

Raumedic AG manufactures reusable and single-use medical devices for intracranial monitoring and catheterization, including intracerebral sensor catheters, pressure-monitoring calibrators, and fixation kits for cranial placement. Their portfolio also includes reusable electrical connection cables for physiological monitors, sterilization/disinfection containers, and subcutaneous tunnellers for device implantation. Additional products cover drill bits for intracerebral catheterization and power adapters for monitoring systems.

The company’s devices are classified under EU Class I and Class II regulations, with listings in the EUDAMED database, FDA’s 510(k) and UDI registries. Their products are designed for invasive neurological monitoring and procedural support, adhering to international medical device compliance frameworks.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue108

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Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
DE-MF-000006155
DUNS number
332785323
EU VAT number
DE231697952
EUDAMED status
Active
EUDAMED registered name
RAUMEDIC AG
Registered address
2, Hermann-Staudinger-Str., 95233, Helmbrechts, Germany
Phone
+49 9252 359-0
PRRC contact
Dr. Gudrun Frohmader(public in EUDAMED)

Frequently asked questions

How many devices does RAUMEDIC AG have in the registry?

The registry currently lists 108 devices for RAUMEDIC AG. Devices recorded under merged duplicate company entries are counted once.

Which registries list RAUMEDIC AG's devices?

Among its 50 most recently registered devices, RAUMEDIC AG has devices listed in EUDAMED (31 devices) and FDA GUDID (23 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do RAUMEDIC AG's devices fall under?

Among its 50 most recently registered devices, the classes recorded for RAUMEDIC AG's devices are Class I, Class IIa, Class IIb and Class II. Each device page shows its own class and authorisation.

What are the newest devices from RAUMEDIC AG in the registry?

The most recently registered devices listed for RAUMEDIC AG include NPS2 Criticare nCompass, LDD - Liquid Dosing Device 5ml Non-Luer, OMNIBAR E5F and Adapter Non-Luer 10 Pack.

Generated automatically from registry data and not verified by a human reviewer.