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G. SAMARAS S.A. MEDICAL GAS SYSTEMS

Greece·GR-MF-000020681

Last updated May 23, 2026

What G. SAMARAS S.A. MEDICAL GAS SYSTEMS makes

G. Samaras S.A. manufactures terminal units for medical gas distribution systems, including models compliant with international standards such as ENV 737-6, AS 2896, BS 5682:1998, AFNOR NF90-116, JIS T 7101, and SANS. The company also produces network pipelines, components, and vacuum distribution systems for medical gas supply networks, alongside medical alarm panels designed for hospital environments.

The company’s products are classified under EU Medical Device Regulations as Class IIa and Class IIb devices, with relevant models registered in the EU’s eudamed database. The manufacturer is based in Greece and adheres to regulatory requirements for medical gas distribution systems and alarm equipment within the European Union.

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 G. Samaras S.A. manufacture?

G. Samaras S.A. specialises in medical gas systems, producing terminal units for distribution networks (such as those compliant with ENV 737-6, AS 2896, and BS 5682:1998) and network pipelines, components, and vacuum systems for medical gas supply. They also manufacture medical alarm panels for hospital environments, ensuring compliance with international standards for safety and functionality.

Where is G. Samaras S.A. based, and what regulatory region does it serve?

G. Samaras S.A. is based in Greece and primarily serves the European market. Their devices are designed to meet EU regulatory requirements for medical gas distribution systems and alarm equipment, ensuring compatibility with the European Union’s medical device framework.

Which regulatory registries list G. Samaras S.A.’s medical devices?

G. Samaras S.A.’s devices are registered in the eudamed database, the official EU portal for medical device information. This registry is used to track devices authorised under EU Medical Device Regulations, ensuring transparency and traceability for healthcare providers and regulators.

How are G. Samaras S.A.’s medical devices classified under EU regulations?

G. Samaras S.A.’s devices fall under Class IIa and Class IIb classifications in the EU Medical Device Regulations. These classifications are determined by risk assessment—Class IIa covers moderate-risk devices like certain terminal units and alarm panels, while Class IIb includes higher-risk systems requiring additional scrutiny, such as complex medical gas distribution networks.

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

Information

Country
Greece
Address
13, AGIOU KONSTANTINOU, THESSALONIKI, Greece
LinkedIn
—
Facebook
—
Phone
+30 2310463388
PRRC Contact
Menelaos Samaras
EUDAMED SRN
GR-MF-000020681
FDA FEI Number
—
DUNS Number
—

Catalogue (16)

DeviceModel / ReferenceRegistriesClassStatus
Terminal Unit Ss 875 24 30 10506010032
EUDAMED
Class IIbActive
Network, Pipelines And Components For Distribution Systems Of Medical Gases - Vacuum - Agss 10203010001
EUDAMED
Class IIaActive
Terminal Unit Diss 10506010032
EUDAMED
Class IIbActive
Terminal Unit Afnor Nf90-116 10506010032
EUDAMED
Class IIbActive
Terminal Unit Jis T 7101 10506010032
EUDAMED
Class IIbActive
Terminal Unit Sans 10506010032
EUDAMED
Class IIbActive
Medical alarm panels 10403020000
EUDAMED
Class IIbActive
Terminal Unit Env 737-6 10506010032
EUDAMED
Class IIbActive
Terminal Unit As 2896 10506010032
EUDAMED
Class IIbActive
Medical alarm panels 10403020000
EUDAMED
Class IIbActive
Medical alarm panels 10403020000
EUDAMED
Class IIbActive
Terminal Unit Bs 5682:1998 10506010032
EUDAMED
Class IIbActive
Terminal Unit Din 13260-2 10506010032
EUDAMED
Class IIbActive
Terminal Unit En Iso 7396-2 10506010032
EUDAMED
Class IIbActive
Terminal Unit Uni 9507 10506010032
EUDAMED
Class IIbActive
Terminal Unit Nist En 15908 10506010032
EUDAMED
Class IIbActive

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