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Device Explorer · FDA GUDID · GMDN 66374

Carbon dioxide low pressure hose

"A length of reinforced colour-coded flexible tubing produced according to ISO5359 and intended to conduct compressed carbon dioxide (CO2) from a CO2 terminal unit or CO2 cylinder to a medical device that functions with CO2 (e.g., ventilator, insufflation syst

US‑registered devices264in commercial distribution
Companies4labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription97%Rx‑only share
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Share of device records

Ohio Medical, Llc19072%
Western Enterprises6223%
Gentec(Shanghai)Corporation83%
Dehas Medical Systems Gmbh42%

Top labelers

CompanyDevicesShare
Ohio Medical, Llc19072%
Western Enterprises6223%
Gentec(Shanghai)Corporation83%
Dehas Medical Systems Gmbh42%

Company = labeler of record on GUDID. 4 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

GENTEC®Quality ConnectOhioWestern/Scott Fetzer

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
BYXTUBING, PRESSURE AND ACCESSORIES194
BYXTubing, Pressure And Accessories80

GMDN & GCC registration

  • GMDN code 66374 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 97% · OTC 3%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

No structured size data on the register.

Use these as the dimensions to specify in a tender line.

How many carbon dioxide low pressure hose products are registered in the US?

264 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Carbon dioxide low pressure hose", from 4 companies. The largest labeler is Ohio Medical, Llc with 72% of records.

Which FDA product codes apply?

BYX (TUBING, PRESSURE AND ACCESSORIES), BYX (Tubing, Pressure And Accessories)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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