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BMED SRL

Italy·IT-MF-000030690

Last updated September 18, 2026

About

Browse our Surgery Tools catalog. Production and sale of superior surgical instruments exclusively made with the best German martensitic steels.

Translated from the manufacturer's own website. Source

What BMED SRL makes

BMED SRL manufactures surgical instruments, including models such as the FM-1, FM-2, and FM-3, designed for medical procedures. These tools are crafted from martensitic steels, a material known for its durability and precision in surgical applications.

The company’s products fall under EU Class I medical devices and are registered in the EU’s eudamed database. BMED SRL is based in Italy and adheres to EU regulatory requirements for these devices.

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 BMED SRL manufacture?

BMED SRL specializes in surgical instruments, including models like the FM-1, FM-2, and FM-3. These tools are crafted from martensitic steels, a material chosen for its strength and precision in medical procedures. The focus is on high-quality surgical tools designed for reliability during operations.

Where is BMED SRL based, and what regulatory framework does it follow?

BMED SRL is based in Italy. Its devices are classified under EU Class I, meaning they pose minimal risk and are subject to the EU’s medical device regulations. Compliance with these rules ensures their safety and performance meet EU standards for medical instruments.

Are BMED SRL’s devices listed in any regulatory registries?

Yes, BMED SRL’s devices are registered in the eudamed database, the official EU portal for medical device information. This listing confirms their compliance with EU regulatory requirements and provides transparency for healthcare professionals and authorities.

How are BMED SRL’s devices classified, and why does this matter?

BMED SRL’s devices fall under EU Class I, the lowest risk category for medical devices. This classification means they undergo fewer regulatory checks than higher-risk devices but still must meet basic safety and performance standards. Class I devices are typically non-invasive and pose minimal risk, such as surgical instruments.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Italy
Address
166, MINCIO, SAN GIOVANNI IN MARIGNANO (RN), Italy
LinkedIn
—
Facebook
—
Phone
+39 05411799990
PRRC Contact
MARCO GALVANI
EUDAMED SRN
IT-MF-000030690
FDA FEI Number
—
DUNS Number
—

Catalogue (3)

DeviceModel / ReferenceRegistriesClassStatus
Fm-3 FM-3
EUDAMED
Class IActive
Fm-1 FM-1
EUDAMED
Class IActive
Fm-2 FM-2
EUDAMED
Class IActive

Related Companies

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