BEHRINGER S.R.L.
Italy IT-MF-000023450 Last updated 17 Sep 2026
- Devices
- 3,319
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Rid. Fc/Dslt 05 O2(Din-9) Din-G 1/4 Ref HR324OXNG05G2
Regolatore Rvb 1000 A.barra Din Ref HR084A
Imp Amb O2 3UNI Rid Afn Man 2, 5 Comp Ref HKAMB045
DOSALITRI Air 30 RAIL - SS - G1/4 Ref HD091
FLUX Mix1 15 CW RAIL - BS - G1/4 Ref HF282B
Dosalitri O2 30 - Uni - 9/16 Ref HD187
DOSALITRI Air 30 RAIL - DIN - G1/4 Ref HD089
Rid. Fc/Flux 30 O2(Din-13) - G 1/4 Ref HR310OXBF30G2
DUAL DSLT Air 15+30 - G1/4 - 9/16 Ref HD420
FLEX 2, 5m O2 I AFN 90 ° - I NST 180 ° Ref HT25OX9IAF8INI
REGOLATORE RVB 600 DIN BEH - 150cc Ref HR085C
Valvola Area P/Avb N2O Nist Ref HG170NOPENST
RID. FC/DSLT 30 Air400(BS-3) BS-3/8 Ref HR323AIAB30G4
INNESTO UNI BEH Vac D8 Ref HI012
Presa Din CO2 1/4"M Ref HP049D
PRESA BS Air400 1/4"M Ref HP165
Flux O2 5 Cw - Din - G1/4 Ref HF204
Innesto A Portagomma Ss Agss Ref HI112SSSS
FLEX 5, 0m N2O I AFN 180 ° - I AFN 90 ° Ref HT50ND8IAF9IAF
Riduttore Hf/200 N2O(Ind) D6 Ref HR186
DUAL FLUX O2 15+15 Al RAIL - SS - G1/4 Ref HF146A
Presa Nist Iso 18082 N2O Ref HP123
FLUX Mix1 5 Al RAIL - BS - G1/4 Ref HF261B
DOSALITRI Air 5 - AFN - 9/16 Ref HD212
INNESTO SS Ar 90° D6 Ref HI120SSAR
PRESA LEAF AFNOR O2 93 Tedisel Ref HP301AFO9TED
Rid. Fc N2(CGA580) - G1/4 Ref HR300N4AHG2
Blocco Base Din/Bs N2O D6 Ref HP235
Presa Leaf Ss CO2 Beh Ref HP301SSCDBEH
Quadro Iii Fonte Gigant/R CO2 Ref HQ128
DUAL DSLT Air 15+15 - BS - 3/8 Ref HD364
INNESTO NIST ISO 18082 Vac D8 Ref HI090
RID. FC/DSLT 30 Air400(UNI-6) AFN-G 1/4 Ref HR322AIOB30G2
Presa Uni Beh O2 1/4"M Ref HP030
BLOCCO BASE DIN/BS Vac D8 Ref HP237
FLUX ELITE O2 15 Al - BS - 9/16 Ref HF089G
Innesto Din N2O D6 Ref HI064A
QUADRO ECO/4 EVO III-F H.F. Air 7, 5bar T Ref HQ067AI08KT
Dosalitri O2 30 - Afn - 9/16 Ref HD188
RID. FC/DSLT 15 Air400(NF-D) AFN-G 1/4 Ref HR322AIM215G2
Riduttore Hf/200 O2(F-Ind) D6 Ref HR127
FLUX HUMI O2 15 Al - SS -D6 Ref HF161A
Sdoppiatore Prese Uni O2 | Barra Ref HP059BAR
Flux O2 15 Cw - Din - G1/4 Ref HF211
FLUX Mix1 15 CW - UNI - G1/4 Ref HF279
RID. FC/FLUX 05 Air400(NF-F) - G 1/4 Ref HR310AIM605G2
Flex Inox - MT.1 - N2 (D) Ref HS077MT1N26
DOSALITRI Air 5 - G1/4 - M12 Ref HD109
GRUPPO II°STADIO EN 7396-1 Air800 UNI Ref HG160A8UNI
Imp Amb O2 3AFN Norid E-Afn I-Man Ref HKAMB009N0012530AFAA
Showing 1-50 of 3,319
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