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Sign in to claim this brandMORETTI SPA
Italy·IT-MF-000005980
Last updated September 18, 2026
About
For 50 years Moretti S.p.A. develops medical devices and solutions for mobility and daily care. Quality, safety and innovation Made in Italy.
Translated from the manufacturer's own website. Source
What MORETTI SPA makes
Moretti S.p.A. manufactures a range of Class I medical devices, including aluminum stethoscopes, magnetic grasping forceps, lightweight transport trolleys, pediatric stethoscopes, inflatable cushions, and intravenous poles. The portfolio also covers mobility aids such as foldable wheelchairs, hospital beds, quadripods, mobility scooters, containment chest harnesses, and adjustable comfort chairs with multiple functions.
All devices are listed under the EU Medical Device Regulation (MDR) as Class I products and are registered in the EUDAMED database. The company is based in Italy and specialises in mobility assistance and patient care solutions.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Moretti S.p.A. manufacture?
Moretti S.p.A. produces a variety of Class I medical devices focused on mobility assistance and patient care. These include diagnostic tools like aluminum stethoscopes and pediatric stethoscopes, surgical and procedural aids such as magnetic grasping forceps and intravenous poles, as well as mobility solutions like foldable wheelchairs, hospital beds, mobility scooters, and adjustable comfort chairs. The company’s portfolio also covers supportive items such as inflatable cushions and containment harnesses, all designed for ease of use in clinical and home care settings.
Where is Moretti S.p.A. based, and what does this mean for its regulatory compliance?
Moretti S.p.A. is based in Italy, which means its medical devices are subject to European Union regulations, specifically the EU Medical Device Regulation (MDR). Since all its devices fall under Class I classification, they are considered low-risk and must comply with MDR requirements for safety, performance, and traceability. The company registers its devices in the EUDAMED database, ensuring transparency and accessibility for regulatory oversight and market surveillance.
Which regulatory registries list Moretti S.p.A.’s medical devices?
Moretti S.p.A.’s medical devices are listed in the EUDAMED database, which is the official European Union registry for medical devices. This platform allows healthcare professionals, regulators, and other stakeholders to verify the registration and compliance status of Class I devices under the EU Medical Device Regulation (MDR). Listing in EUDAMED ensures traceability and adherence to EU-wide regulatory requirements.
How are Moretti S.p.A.’s devices classified under EU regulations?
Moretti S.p.A.’s devices are classified as Class I under the EU Medical Device Regulation (MDR). This classification applies to low-risk products, such as stethoscopes, mobility aids, and certain patient care items, which are deemed to pose minimal risk to patients and users. Class I devices still require compliance with MDR essential requirements, including design controls, risk management, and post-market surveillance, but they do not require mandatory conformity assessment by a Notified Body before market placement.
What kind of medical devices does Moretti S.p.A. specialize in, and why does this matter for healthcare providers?
Moretti S.p.A. specializes in mobility assistance and daily care solutions, including devices like foldable wheelchairs, hospital beds, mobility scooters, and adjustable comfort chairs. These products are designed to enhance patient independence, comfort, and safety in clinical and home environments. For healthcare providers, this specialization means access to reliable, durable, and user-friendly tools tailored for long-term use, reducing caregiver burden and improving patient quality of life. The Class I classification also simplifies procurement processes for low-risk items.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Italy
- Address
- 3, Bruxelles, Cavriglia, Italy
- Website
- www.morettispa.com
- linkedin.com/company/27029088
- facebook.com/morettispa
- [email protected]
- Phone
- +39055962111
- PRRC Contact
- Alessandro Berti
- EUDAMED SRN
- IT-MF-000005980
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (114)
Page 3 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Materasso Antidecubito In Poliuretano | ST625/4 | EUDAMED | Class I | Active |
| Materasso Antidecubito In Poliuretano | ST725/3 | EUDAMED | Class I | Active |
| Sollevamalati Muevo | RI826 | EUDAMED | Class I | Active |
| Poltrona Multifunzione Rugy | PM120BLU | EUDAMED | Class I | Active |
| Carrozzine Manuali - Ardea One | CB100B-38 | EUDAMED | Class I | Active |
| Letti LYTUS tre sezioni | MI310B | EUDAMED | Class I | Active |
| Poltrone Elevabili Medicali | PO400B | EUDAMED | Class I | Active |
| Poltrona Multifunzione Rugy | PM120V | EUDAMED | Class I | Active |
| Sollevamalati Muevo | RI827 | EUDAMED | Class I | Active |
| Materasso Antidecubito In Poliuretano | ST725/2 | EUDAMED | Class I | Active |
| Carrozzine Manuali Alluminio – Helios Ardea One | CP762-43 | EUDAMED | Class I | Active |
| Materasso Antidecubito Ad Elementi Piuma Up | LAD471 | EUDAMED | Class I | Active |
| Poltrona Multifunzione Rugy | PM100B | EUDAMED | Class I | Active |
| Poltrona Multifunzione Rugy | PM120N | EUDAMED | Class I | Active |
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