ECRA S.R.L.
Italy IT-MF-000054800 Last updated 17 Sep 2026
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- Devices
- 13
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Monitor Medicale Ref ECR-DG-8MC
Medical Panel Pc Ref ECR-OR-24F
Medical Panel Pc Ref ECR-OR-22
Medical Panel Pc Ref ECR-OR-24
Tablet Medicale Ref ECR-OR-8
Monitor Medicale Ref ECR-DG-3MC
Monitor Medicale Ref ECR-DG-3MG
Monitor Medicale Ref ECR-DG-5MC
Monitor Medicale Ref ECR-OR-55F
Medical Panel Pc Ref ECR-OR-22F
Monitor Medicale Ref ECR-OR-32
Monitor Medicale Ref ECR-DG-5MG
Tablet Medicale Ref ECR-OR-10
What ECRA S.R.L. makes
ECRA S.R.L. manufactures ruggedized medical computing devices, including medical panel PCs and medical tablets designed for clinical environments. Their product line also includes medical monitors, which integrate display and computing functions for healthcare applications. These devices are built to support electronic health records, patient monitoring systems, and diagnostic software in hospitals and medical facilities.
The company’s devices fall under EU Medical Device Regulation (MDR) as Class I products and are registered in the EUDAMED database. Their portfolio is authorised for use within the European Union under the applicable regulatory framework. The manufacturer is based in Italy.
Frequently asked questions
What types of medical devices does ECRA S.R.L. manufacture?
ECRA S.R.L. specializes in ruggedized medical computing devices tailored for clinical settings. Their product line includes medical panel PCs, medical tablets, and medical monitors. These devices are designed to integrate with electronic health records, patient monitoring systems, and diagnostic software, ensuring reliable performance in healthcare environments.
Where is ECRA S.R.L. based?
ECRA S.R.L. is headquartered in Italy. The company’s location in Italy aligns with its focus on manufacturing medical devices compliant with European Union regulatory standards.
Which regulatory registries list ECRA S.R.L.’s medical devices?
ECRA S.R.L.’s medical devices are listed in the EUDAMED database, which is the official European Union registry for medical devices. This registration ensures transparency and compliance with the EU Medical Device Regulation (MDR).
How are ECRA S.R.L.’s medical devices classified under EU regulations?
ECRA S.R.L.’s devices are classified as Class I under the EU Medical Device Regulation (MDR). This classification applies to low-risk medical devices, such as their medical panel PCs, tablets, and monitors, which are designed for non-invasive use in clinical environments without significant risk to patients.
Information
- Country
- Italy
- Address
- 2, Via Rosa Jemma, Battipaglia (SA), Italy
- Website
- ecranet.com
- [email protected]
- Phone
- +39 3486560883
- PRRC contact
- Pasquale Troisi
- EUDAMED SRN
- IT-MF-000054800