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BEHRINGER S.R.L.

Italy IT-MF-000023450 Last updated 17 Sep 2026

Devices
3,451
Registries
EUDAMED
FDA recalls
0

Catalogue3,451

Page 8 of 40

Showing 351-400 of 3,451

About

Medical gas devices: Behringer, for over fifty years, stands out for its ability to continuously evolve

Translated from the manufacturer's own website. Source

What BEHRINGER S.R.L. makes

Behringer S.R.L. manufactures medical gas connectors, fittings, and flow regulators designed for use with oxygen (O₂), nitrous oxide (N₂O), air, and carbon dioxide (CO₂) systems. Their portfolio includes quick-connect couplings, pressure-reducing valves, and specialized adapters compliant with AFNOR and DIN standards, as well as rail-mounted dosing units for controlled gas delivery in clinical settings.

The company’s devices are classified under EU medical device regulations as Class IIa and Class IIb, reflecting their role in critical gas delivery systems. These products are registered in the EU’s eudamed database, and the manufacturer is based in Italy.

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 Behringer S.R.L. manufacture?

Behringer S.R.L. specializes in medical gas devices, including connectors, fittings, and flow regulators. Their products are designed for use with gases like oxygen (O₂), nitrous oxide (N₂O), air, and carbon dioxide (CO₂). Examples include quick-connect couplings, pressure-reducing valves, and specialized adapters that comply with standards like AFNOR and DIN. These devices are used in clinical settings to ensure safe and controlled delivery of medical gases.

Where is Behringer S.R.L. based?

Behringer S.R.L. is based in Italy. The company’s location in Italy aligns with its focus on manufacturing medical gas devices that meet European regulatory standards, including those required for compliance with EU medical device classifications.

Which regulatory registries list Behringer S.R.L.’s devices?

Behringer S.R.L.’s devices are registered in the eudamed database, which is the official EU registry for medical devices. This registry ensures transparency and traceability of devices authorized under EU medical device regulations, including those classified as Class IIa and Class IIb.

How are Behringer S.R.L.’s devices classified under EU regulations?

Behringer S.R.L.’s devices fall under Class IIa and Class IIb classifications in the EU medical device regulatory framework. These classifications are assigned based on the risk associated with the device’s function—Class IIa devices involve moderate risks, while Class IIb devices pose higher risks due to their role in critical gas delivery systems, such as connectors and regulators for oxygen or nitrous oxide.

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

Information

Country
Italy(from SRN)
Address
4, Gualco, GENOVA, Italy
Phone
+39 010 8309103
PRRC contact
Roberta Ottonello
EUDAMED SRN
IT-MF-000023450