An assembly of devices designed to conduct medical gases from an anaesthesia unit/workstation to a patient artificial airway/anaesthesia mask (not included) during general anaesthesia. It includes breathing tubes and a Y-piece connector, typically with a venti
| Company | Devices | Share |
|---|---|---|
| Airlife | 1,057 | 31% |
| King Systems Corporation | 636 | 19% |
| Icu Medical, Inc. | 320 | 9% |
| Westmed, Inc. | 298 | 9% |
| Teleflex Incorporated | 188 | 6% |
| Airlife Finland Oy | 182 | 5% |
| Sunmed, Llc | 134 | 4% |
| Flexicare Medical Limited | 107 | 3% |
| Vyaire Medical, Inc. | 66 | 2% |
| Deroyal Industries, Inc. | 49 | 1% |
| Intersurgical Incorporated | 46 | 1% |
| Ventlab, Llc | 38 | 1% |
Company = labeler of record on GUDID. 42 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| CAI | Circuit, breathing (w connector, adaptor, y piece) | 2,110 |
| CAI | Circuit, Breathing (W Connector, Adaptor, Y Piece) | 886 |
| OFP | Anesthesia Breathing Circuit Kit (Adult & Pediatric) | 439 |
| CAH | Filter, Bacterial, Breathing-Circuit | 403 |
| CAH | Filter, bacterial, breathing-circuit | 379 |
| BTC | BAG, RESERVOIR | 320 |
Use these as the dimensions to specify in a tender line.
3,390 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Anaesthesia breathing circuit, single-use", from 42 companies. The largest labeler is Airlife with 31% of records.
CAI (Circuit, breathing (w connector, adaptor, y piece)), CAI (Circuit, Breathing (W Connector, Adaptor, Y Piece)), OFP (Anesthesia Breathing Circuit Kit (Adult & Pediatric)), CAH (Filter, Bacterial, Breathing-Circuit)
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.