BEHRINGER S.R.L.
Italy IT-MF-000023450 Last updated 17 Sep 2026
- Devices
- 3,451
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
FLUX Air 30 Al RAIL - SS - G1/4 Ref HF132A
Presa Afnor Fr O2 D6 Ref HP126
Flex Inox - MT.1 - Air - Type F Ref HS077MT1N13
Dual Dslt O2 15+30 - Afn - M12 Ref HD332
FLUX O2 5 Al RAIL - DIN - 9/16 Ref HF107G
FLUX Air 5 Al - G1/4 - M12 Ref HF090M
UMIDIFICATORE AUTOCLAV. 300cc 9/16" Ref HU009
FLUX O2 30 Al - G1/4 - G1/4 Ref HF080
PRESA LEAF AFNOR Vac TED Ref HP301AFVATED
PRESA NIST ISO 18082 Vac D12 Ref HP225
INNESTO AFNOR VITAEFLO Air400 90° D6 Ref HI021VIT
Imp Amb O2 4UNI Rid Afn E-Afn I-Aut Ref HKAMB010RIAA2510UNDA
Gruppo Ii°stadio En 7396-1 CO2 Nist Ref HG160CDNST
QUADRO ECO/7 EVO N2 9bar F/AUT P Ref HQ066NI09EAP
FLUX Air 30 CW - AFN - G1/4 Ref HF252
Sdoppiatore Prese Uni CO2 | Barra Ref HP328
Dual Dslt O2 15+15 Rail - Bs - 3/8 Ref HD357
RID. FC/FLUX 30 Air400(DIN-6) - G 1/4 Ref HR310AIBA30G2
FLUX ELITE O2 5 Al RAIL - BS - 9/16 Ref HF348B
PRESA VENTURI AGSS 1L REC Tedisel Ref HP304B1LTED
Gruppo Ii°stadio En 7396-1 O2 Nist Ref HG160OXNST
Dual Dslt O2 30+30 - G1/4 - G1/4 Ref HD271
Presa Leaf Ss N2O Arl Ref HP301SSNOARL
Innesto Afnor Ros O2 90° D6 Ref HI020ROS
RID. FC/FLUX 15 Air400(NF-F) - G 1/4 Ref HR310AIM615G2
Valvola Area P/Avb N2O Afnor Ref HG170NOPEAFN
DUAL FLUX O2 15+30 Al RAIL - AFN - G1/4 Ref HF166B
Sdoppiatore Prese Uni CO2 Ref HP327
VALVOLA AREA P/AVB Air400 AFNOR Ref HG170A4PEAFN
UMIDIFICATORE AUTOCLAV. 300cc M12x1, 25 Ref HU008
FLUX Air 30 CW RAIL - BS - G1/4 Ref HF254B
Flex Inox - MT.2 - O2(Bs) Ref HS077MT2N03
Serpentina Rame - MT.1 - CO2(D) Ref HS053D
FLUX Air 30 Al - DIN - G1/4 Ref HF103
PRESA UNI BEH Air400 Ref HP202
INNESTO CZ Air-800 D6 Ref HI123CZA8
Blocco Base Leaf Agss-Side Pipe Ref HP309SSSP
Presa Leaf Bs O2 Gms Ref HP301BSOXGMS
FLUX Air 5 CW - AFN - M12 Ref HF291
BLOCCO BASE DIN/BS Vac 45° Ref HP145L
FLUX Mix1 5 Al RAIL - AFN - M12 Ref HF297B
Blocco Base Agss Flusso Regolabile Ref HP024
DOSALITRI Air 30 - AFN - 9/16 Ref HD236
Regolatore Rvb 1000 D8 Ref HR060PG
Regolatore Rvb 1000 A.barra Din Ref HR084
Serpentina Rame - MT.2 - N2O(Cah) Ref HS065
RIDUTTORE EURO/A Air(F) D6 Ref HR162F
Regolatore Rvb 600 Bs Beh Ref HR090
PRESA LEAF DIN Vac GMS Ref HP301DNVAGMS
Showing 151-200 of 3,451
About
Medical gas devices: Behringer, for over fifty years, stands out for its ability to continuously evolve
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.
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.
Information
- Country
- Italy
- Address
- 4, Gualco, GENOVA, Italy
- Website
- www.behringer.it
- [email protected]
- Phone
- +39 010 8309103
- PRRC contact
- Roberta Ottonello
- EUDAMED SRN
- IT-MF-000023450