OIARSO, S. COOP
Spain Last updated 21 Oct 2026
- Devices
- 598
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Bexen Medical Ref 223.84
Bexen Medical Ref 269.30
Bexen Medical Ref 202.30
Bexen Medical Ref 251.35
Bexen Medical Ref 509.02
Bexen Medical Ref 229.02
Bexen Medical Ref 225.20
Bexen Medical Ref 504.01
Bexen Medical Ref 251.05
Bexen Medical Ref 213.02
Bexen Medical Ref 283.01
Bexen Medical Ref 503.88
Bexen Medical Ref 505.20
Bexen Medical Ref 245.10
Bexen Medical Ref 226.05
Bexen Medical Ref 241.05
Bexen Medical Ref 266.10
Bexen Medical Ref 508.05
Bexen Medical Ref 201.01
Bexen Medical Ref 248.02
Bexen Medical Ref 243.84
Bexen Medical Ref 502.02
Bexen Medical Ref 242.01
Bexen Medical Ref 261.20
Bexen Medical Ref 213.30
Bexen Medical Ref 504.40
Bexen Medical Ref 545.05
Bexen Medical Ref 226.01
Bexen Medical Ref 511.20
Bexen Medical Ref 296.13
Bexen Medical Ref 283.10
Bexen Medical Ref 534.30
Bexen Medical Ref 261.30
Bexen Medical Ref 201.05
Bexen Medical Ref 264.40
Bexen Medical Ref 243.20
Bexen Medical Ref 901.07
Bexen Medical Ref 228.01
Bexen Medical Ref 242.20
Bexen Medical Ref 506.02
Bexen Medical Ref 505.40
Bexen Medical Ref 244.20
Bexen Medical Ref 264.10
Bexen Medical Ref 269.02
Bexen Medical Ref 517.05
Bexen Medical Ref 236.31
Bexen Medical Ref 501.05
Bexen Medical Ref 210.05
Bexen Medical Ref 503.90
Bexen Medical Ref 206.30
Showing 201-250 of 598
EUDAMED certificates
Notified body 0318 1 certificate
- 2023 PR 0007 Supplemented
Quality assurance EU MDR
- Issued
- 8 Oct 2026
- Expires
- 5 Nov 2028
- Reason
- Add device or group
Related companies
Notified bodies
- Notified body 0318
About
Leaders in medical material, hospital products, defibrillators and https: / / bexen.com / wp-content / uploads / logo-bexen.svgmanagement of biological samples and medicines.
What OIARSO, S. COOP makes
Oiarso manufactures a range of medical devices under the Bexen brand, including defibrillators and hospital products. Their portfolio also includes materials and tools for managing biological samples and medicines, as well as medical materials for clinical and hospital use.
The company’s devices are classified under EU Medical Device Regulations as Class I, Class IIa, and Class IIb. These products are listed in the EU’s eudamed registry, and the manufacturer is based in Spain.
Information
- Address
- 57-F, Bº ZIKUÑAGA, HERNANI, Spain
- Website
- www.bexenmedical.com/
- [email protected]
- Phone
- +34 943 33 50 20
- PRRC contact
- GORKA RAMÍREZ GONZÁLEZ
- EUDAMED SRN
- ES-MF-000000866