Medaxis AG
Active in EUDAMEDSwitzerlandfrom SRN EUDAMED FDA SRN CH-MF-000011487 FEI 3014118821
Medaxis AG is a medical device manufacturer based in Switzerland, with 18 devices listed in FDA GUDID and EUDAMED (FDA Class II; EU Class I) as of 13 Nov 2026.
- Devices
- 18
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 17
- EUDAMED 2
- Device classes
- FDA Class II 16
- EU Class I 2
- Top EMDN categories
- Sites and related companies
- Emergo Europe B.V. authorised representative
- Identifiers
- EUDAMED SRN CH-MF-000011487
- FDA FEI 3014118821
- DUNS 480870674
At a glance
EU certificates
1 of 1 in force.
Market reach
- European Union
- EUDAMED actor, 1 certificate
- United States
- FDA FEI
- Authorised rep.
- Emergo Europe B.V.NL
What Medaxis AG makes
Medaxis AG manufactures surgical irrigation system nozzles and surgical/orthopaedic lavage control units, including specific products such as the debritom+ series and the AeroGuard 'Nebbia' and AeroGuard 'Jellyfish' devices.
These devices are classified as Class I and Class II medical devices and are listed in the EUDAMED and FDA UDI registries; the company is based in Switzerland (CH).
Catalogue
Search and filter all 18 devicesCompany details
- EUDAMED SRN
- CH-MF-000011487
- FDA FEI number
- 3014118821
- DUNS number
- 480870674
- EU VAT number
- CHE-107.902.358
- EUDAMED status
- Active
- EUDAMED registered name
- medaxis AG
- Registered address
- 9, Bahnhofstrasse, 6340, Baar, Switzerland
- Website
- medaxis.ch/de.html
- info@medaxis.ch
- Phone
- +41 62 823 88 00
- PRRC contact
- Daniel Fehr
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 1 Jun 2027
TÜV SÜD Product Service GmbH 0123 1 certificate
- G10 092556 0006 Expiring
Quality management system EU MDR
- Issued
- 19 Mar 2025
- Expires
- 1 Jun 2027
Frequently asked questions
How many devices does Medaxis AG have in the registry?
The registry currently lists 18 devices for Medaxis AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medaxis AG's devices?
Among its 18 most recently registered devices, Medaxis AG has devices listed in EUDAMED (2 devices) and FDA GUDID (17 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Medaxis AG's devices fall under?
Among its 18 most recently registered devices, the classes recorded for Medaxis AG's devices are Class I and Class II. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Medaxis AG?
EUDAMED lists 1 certificate for Medaxis AG (quality management system) under MDR. 1 is recorded with the status issued. The most recent was issued on 19 Mar 2025.
What are the newest devices from Medaxis AG in the registry?
The most recently registered devices listed for Medaxis AG include debritom+ 1000.0501, debritom+ 1000.0500, debritom+ 1000.0006 and debritom+ 2000.0201.