A hollow cylinder that is designed for oral insertion via the trachea and into a lung to maintain airway patency and/or to deliver anaesthetic inhalation agents or other medical gases, and secure ventilation. It is typically made of plastic, rubber, or silicon
| Company | Devices | Share |
|---|---|---|
| Covidien Lp | 75 | 22% |
| Teleflex Incorporated | 71 | 21% |
| Fuji Systems Corporation | 38 | 11% |
| Medline Industries, Inc. | 22 | 6% |
| Henan Tuoren Medical Device Co.,Ltd. | 18 | 5% |
| Salter Labs | 18 | 5% |
| Insung Medical Co., Ltd.. | 16 | 5% |
| Hangzhou Tappa Medical Technology Co., Ltd. | 12 | 4% |
| Well Lead Medical Co.,Ltd | 12 | 4% |
| Forsure Medical Products Llc | 12 | 4% |
| Icu Medical, Inc. | 12 | 4% |
| Cook Incorporated | 11 | 3% |
Company = labeler of record on GUDID. 15 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 |
|---|---|---|
| CBI | Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Con | 134 |
| CBI | TUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CON | 89 |
| BTS | TUBE, BRONCHIAL (W/WO CONNECTOR) | 50 |
| BYE | Attachment, breathing, positive end expiratory pressure | 30 |
| BTR | Tube, tracheal (w/wo connector) | 22 |
| OFP | Anesthesia Breathing Circuit Kit (Adult & Pediatric) | 10 |
Use these as the dimensions to specify in a tender line.
No closely related category with 50+ devices.
339 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Endobronchial tube", from 15 companies. The largest labeler is Covidien Lp with 22% of records.
CBI (Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Con), CBI (TUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CON), BTS (TUBE, BRONCHIAL (W/WO CONNECTOR)), BYE (Attachment, breathing, positive end expiratory pressure)
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.