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Cardiovascular Instruments Manufacturers in Spain

4 cardiovascular instruments manufacturers in Spain are listed in this directory. All of them are based in Spain. Main locations: Cerdanyola del Vallès, Hernani, Lliçà de Vall, Sant Vicenç dels Horts. Each profile shows the business type, product categories and official contact details published by the company; use the filters to narrow the list.

4 companies

Bexen Medical

Hernani, Spain

ManufacturerDistributorEstablished 1978

Basque cooperative group manufacturing and distributing medical supplies and defibrillators since 1978.

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IHT – Iberhospitex

Lliçà de Vall, Spain

Manufacturer

Catalan company developing, manufacturing and marketing medical devices.

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iVascular

Sant Vicenç dels Horts, Spain

ManufacturerEstablished 2010

Barcelona-area company founded in 2010 that develops and produces stents and catheters for endovascular treatment.

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NEOS Surgery

Cerdanyola del Vallès, Spain

ManufacturerEstablished 2003

Barcelona-area developer and manufacturer of cranial and sternal closure devices for neurosurgery and cardiothoracic surgery, founded in 2003.

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Questions about Cardiovascular Instruments Manufacturers in Spain

How many Cardiovascular Instruments manufacturers in Spain are listed?

4 companies match this category and country as a manufacturer. The list updates automatically when profiles are added or changed.

How are the companies listed?

Profiles are compiled from each company’s own website and public sources; verified details are marked on the profile. Featured or Sponsored labels are paid placements, not endorsements. See how listings are checked.

How do I contact a company?

Open the company profile for its official website, e-mail and phone details, and contact the company directly. SurgiFacts.com does not sell instruments.

Business types in Spain

Cities in Spain

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Medical exhibitions in Spain

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Verified specialties in Spain

Regulation in Spain

Spain is in the EU / EEA, so the EU framework applies.

Regulator: European Commission (DG SANTE) with national competent authorities of EU/EEA Member States

Two EU regulations govern medical devices and IVDs in the EU/EEA; devices need CE marking after the conformity assessment route set by their risk class.

From the sourced EU MDR / IVDR entry, checked 29 October 2026. General information, not legal advice. Requirements for Spain · All medical certifications

Frequently asked questions

What does a Spanish company take on when it acts as EU authorized representative?

A non-EU manufacturer must designate a single EU authorized representative by written mandate (Article 11 of the EU MDR), and an EU company, for example one in Spain, can take on that role. The authorized representative must:

  • check that the Declaration of Conformity and technical documentation exist and keep copies available to authorities;
  • register in EUDAMED and cooperate on corrective actions and incidents;
  • have a PRRC available;
  • end the mandate and inform the authority if the manufacturer breaches its obligations.

The authorized representative's details appear on the labeling. It is not automatically the importer or distributor. Browse Spanish companies on the Spain country page.

Spain

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