BEHRINGER S.R.L.
Italy IT-MF-000023450 Last updated 17 Sep 2026
- Devices
- 3,451
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Presa Leaf Din N2O Lm Ref HP301DNNOLMM
Riduttore Hf O2(Hr) Afnor/Amb/Trasd. Ref HR244
Imp Amb O2 4DIN Norid I-Aut Ref HKAMB010N0012530DNB2
Gruppo Ii°stadio En 7396-1 CO2 (F) Ref HG084F
Regolatore Rvb 250 Bs Beh Ref HR089
Innesto Uni Beh N2O D6 Ref HI013
Regolatore Rvb 600 Din Beh Ref HR085
PRESA AFNOR FR Air800 1/4"M Ref HP193
Rid. Fc/Flux 30 O2(CGA540) - 9/16 Ref HR310OXAG30U1
Rid. Fc O2(Bs-3) - 3/8 Ref HR300OXABG4
Dosalitri O2 30 - G1/4 - 3/8 Ref HD127
Riduttore Hf/P O2 Innesto Uni Ref HR142
FLEX 1, 0m O2 I AFN 180 ° - G1/4"F 180 ° Ref HT10OX8IAF8FF4
DOSALITRI Air 50 - SS - G1/4 Ref HD076
Imp Amb O2 4UNI Norid E-Afn I-Aut Ref HKAMB010N00A2530UNBA
Rid. Fc/Dslt 30 O2(Uni-2) Uni-9/16 Ref HR327OXOD30U1
RID. FC/FLUX 15 Air400(NF-D) - G 1/4 Ref HR310AIM215G2
FLUX ELITE O2 5 Al - AFN - 9/16 Ref HF346
Dual Dslt O2 30+30 Rail - Bs - G1/4 Ref HD291
Rid. Fc/Flux 30 O2(Bs-3) - 3/8 Ref HR310OXAB30G4
Connessione Rame - Mt. 0, 5 - Air Ref HS028D
DUAL FLUX O2 15+30 Al - DIN - G1/4 Ref HF167D
Riduttore Hf N2(I) Presa Uni Ref HR037
PRESA LEAF SS Ar TED Ref HP301SSARTED
Presa Leaf Afnor CO2 Ted Ref HP301AFCDTED
FLUX Air 15 CW - G1/4 - G1/4 Ref HF242
Presa Leaf Afnor N2O Nov Ref HP301AFNONOV
Flux O2 15 Cw - G1/4F - 3/8 Ref HF367
PRESA LEAF SS Air800 ULC Ref HP301SSA8ULC
DOSALITRI Air 5 - DIN - 9/16 Ref HD213
Innesto Cz O2 93 1/4" F Ref HI121CZO9
Rid. Fc N2O(Nf-G) - 9/16 Ref HR300NOM3U1
Rid. Fc N2(Nf-F) - 9/16 Ref HR300N4M6U1
GRUPPO II°STADIO EN 7396-1 Air400 UNI Ref HG160A4NAUNI
Valvola Di Servizio DN15 PN20 D14 Ref H0672C
Msa N2O Afn Ref HG150NOAFN
DUAL FLUX Air 15+30 Al - SS - G1/4 Ref HF181D
BLOCCO BASE DIN/BS Air800 Ref HP270A8
Innesto Nist Iso 18082 O2 1/4"F Ref HI080
Rid. Fc N2O(Din-6) - Afn Ref HR300NOBAAF
Innesto Uni Beh O2 90° D6 Ref HI026
Rid. Fc/Dslt 15 O2(Nf-F) Din-3/8 Ref HR324OXM615G4
Flux O2 5 Cw Rail - Bs - 9/16 Ref HF327B
PRESA NIST ISO 18082 Vac D8 Ref HP219
Gruppo Ii°stadio En 7396-1 O2-93 Afnor Ref HG160O9AFN
Gruppo Ii°stadio En 7396-1 N2 Uni Ref HG160N4NAUNI
FLEX 2, 0m Air400 I NST 180 ° - P NST 180 ° Ref HT20M48INI8PNI
DUAL FLUX Air 15+30 Al RAIL - UNI - G1/4 Ref HF177B
DUAL DSLT Air 15+30 - AFN - 9/16 Ref HD423
DUAL FLUX O2 30+30 Al - UNI - 9/16 Ref HF171E
Showing 301-350 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