A hollow cylinder inserted orally or nasally into the trachea to provide an unobstructed airway to convey gases and vapours to and from the lungs during anaesthesia, resuscitation, and other situations where the patient is not properly ventilated; it does not
| Company | Devices | Share |
|---|---|---|
| Icu Medical, Inc. | 37 | 64% |
| Teleflex Incorporated | 18 | 31% |
| Boss Instruments, Ltd., Inc. | 3 | 5% |
Company = labeler of record on GUDID. 3 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 |
|---|---|---|
| BTR | Tube, tracheal (w/wo connector) | 55 |
| KTI | BRONCHOSCOPE ACCESSORY | 6 |
| KCB | TUBE, TONSIL SUCTION | 3 |
| EOQ | BRONCHOSCOPE (FLEXIBLE OR RIGID) | 2 |
| BZA | Connector, Airway (Extension) | 1 |
Use these as the dimensions to specify in a tender line.
58 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Basic endotracheal tube, reusable", from 3 companies. The largest labeler is Icu Medical, Inc. with 64% of records.
BTR (Tube, tracheal (w/wo connector)), KTI (BRONCHOSCOPE ACCESSORY), KCB (TUBE, TONSIL SUCTION), EOQ (BRONCHOSCOPE (FLEXIBLE OR RIGID))
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.