A sterile flexible tube designed for periodic tracheal and pharyngeal mucus aspiration and inflation of the lungs with a flow of gas from its distal tip. It consists of a single lumen tube for alternating suction and insufflation. This is a single-use device.
| Company | Devices | Share |
|---|---|---|
| Airlife | 59 | 53% |
| Icu Medical, Inc. | 38 | 34% |
| Dynarex Corporation | 13 | 12% |
| Hobbs Medical, Inc. | 1 | 1% |
Company = labeler of record on GUDID. 4 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 |
|---|---|---|
| BSY | CATHETERS, SUCTION, TRACHEOBRONCHIAL | 50 |
| CAF | NEBULIZER (DIRECT PATIENT INTERFACE) | 38 |
| BSY | Catheters, Suction, Tracheobronchial | 29 |
| OFO | Airway suction kit | 11 |
| OFO | Airway Suction Kit | 7 |
| OFP | Anesthesia breathing circuit kit (adult & pediatric) | 6 |
Use these as the dimensions to specify in a tender line.
111 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Tracheobronchial suction/insufflation catheter, single-lumen", from 4 companies. The largest labeler is Airlife with 53% of records.
BSY (CATHETERS, SUCTION, TRACHEOBRONCHIAL), CAF (NEBULIZER (DIRECT PATIENT INTERFACE)), BSY (Catheters, Suction, Tracheobronchial), OFO (Airway suction kit)
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.