Medartis AG
Active in EUDAMEDSwitzerlandfrom SRN EUDAMED FDA SRN CH-MF-000022291 FEI 3003236702
Medartis AG is a medical device manufacturer based in Switzerland, with 5,186 devices listed as of 12 Nov 2026.
- Devices
- 5,186
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- EUDAMED 2,998
- FDA GUDID 2,631
- FDA 510(k) 2
- Device classes
- EU Class IIb 2,289
- EU Class I 576
- EU Class IIa 133
- FDA Class II 2
- Top EMDN categories
- Orthopaedic prostheses, osteosynthesis devices, devices for tendon and ligament synthesis 2,288
- Various devices not included in other classes 502
- Instruments for functional explorations and therapeutic interventions 132
- Surgical instruments, reusable - other 39
- Orthopaedic and traumatological surgery instruments, reusable 36
- Medical device software - not included in other classes 1
- Sites and related companies
- Medartis GmbH authorised representative
- Identifiers
- EUDAMED SRN CH-MF-000022291
- FDA FEI 3003236702
- DUNS 480054895
At a glance
EU certificates
1 of 1 in force.
Market reach
- European Union
- EUDAMED actor, 1 certificate
- United States
- FDA FEI
- Authorised rep.
- Medartis GmbHDE
What Medartis AG makes
Medartis AG produces reusable surgical implant templates, orthopaedic fixation hardware (including non-sliding bone screws and non-bioabsorbable plates), orthodontic tubes, surgical retraction systems, and sterilization/disinfection containers for medical instruments. Their portfolio includes specific orthopaedic plates and screws (e.g., 3.5 PentaLock Prox.Hum. Plate XL), cortical screws (e.g., 1.5mm and 1.2mm), and customisable surgical templates for orthopaedic procedures. Additional items include reusable instrument cases, repositioning hooks, and adhesive stickers for surgical labelling.
The company’s devices are classified under EU Medical Device Regulations as Class I, Class IIa, and Class IIb, with all relevant products listed in the EU’s eudamed database. Medartis AG is headquartered in Switzerland.
Catalogue
Search and filter all 5,186 devicesShowing 1-50 of 5,186
Company details
- EUDAMED SRN
- CH-MF-000022291
- FDA FEI number
- 3003236702
- DUNS number
- 480054895
- EUDAMED status
- Active
- EUDAMED registered name
- Medartis AG
- Registered address
- 60E, Hochbergerstrasse, 4057, Basel, Switzerland
- Phone
- +41 61 633 37 23
- PRRC contact
- Carmen Mangel
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 29 Dec 2026
TÜV Rheinland LGA Products GmbH 0197 1 certificate
- HZ 1809678-1 Expiring
Quality management system EU MDR
- Issued
- 16 Oct 2026
- Expires
- 29 Dec 2026
- Reason
- Other
Frequently asked questions
How many devices does Medartis AG have in the registry?
The registry currently lists 5186 devices for Medartis AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medartis AG's devices?
Among its 50 most recently registered devices, Medartis AG has devices listed in EUDAMED (50 devices).
What risk classes do Medartis AG's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Medartis AG's devices are Class I, Class IIa and Class IIb. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Medartis AG?
EUDAMED lists 1 certificate for Medartis AG (quality management system) under MDR. The most recent was issued on 16 Oct 2026.
What are the newest devices from Medartis AG in the registry?
The most recently registered devices listed for Medartis AG include 1.8 Cortical Screw 12mm, HD4, 5/Pkg, 2.0 SpeedTip Screw 08mm, HD6, 5/Pkg, 1.5 Cortical Screw 07mm, HD4, 4/Pkg and 2.0 Cortical Screw 11mm, HD6, 5/Pkg.