Discover surgical instruments, manufacturers & suppliers, medical exhibitions and industry insights

Diagnostic Instruments Manufacturers in Italy

3 diagnostic instruments manufacturers in Italy are listed in this directory. All of them are based in Italy. Main locations: Vicchio, Trieste, Castenedolo. Each profile shows the business type, product categories and official contact details published by the company; use the filters to narrow the list.

3 companies

Eurospital

Trieste, Italy

Manufacturer

Trieste company producing and marketing pharmaceuticals, medical devices and in-vitro diagnostics.

View profile

FIAB

Vicchio, Italy

Manufacturer

Florence-area manufacturer of cardiac stimulation devices, electrocatheters, ECG electrodes and defibrillation pads.

View profile

Trident Dental

Castenedolo, Italy

Manufacturer

Brescia-area developer and manufacturer of digital imaging and radiology equipment for dentistry.

View profile

Questions about Diagnostic Instruments Manufacturers in Italy

How many Diagnostic Instruments manufacturers in Italy are listed?

3 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 Italy

Cities in Italy

Show all 49 cities

Medical exhibitions in Italy

All 2 upcoming exhibitions in Italy →

Verified specialties in Italy

Regulation in Italy

Italy 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 Italy · All medical certifications

Frequently asked questions

What technical documentation should an Italian manufacturer hold for an MDR instrument?

Every MDR device, including self-declared Class I devices, needs technical documentation under Annexes II and III. For an instrument this usually includes:

  • a device description and specifications, labeling and IFU;
  • a checklist of the General Safety and Performance Requirements, with the standards applied;
  • the risk management file, biocompatibility, sterilization or reprocessing and performance test reports as relevant;
  • a clinical evaluation plan and report, proportionate to risk and updated with post-market data;
  • post-market surveillance documentation.

Buyers rarely receive the full file, but can ask for a summary or the GSPR checklist. Italian manufacturers are on the Italy country page; see the medical certifications page.

Italy

All FAQs