A hollow cylinder designed to be inserted into an artificial opening made in the trachea (windpipe) during a tracheotomy to provide a patent airway; it is not custom-made for a specific patient and is not reinforced with a wire. It is typically constructed of
| Company | Devices | Share |
|---|---|---|
| Icu Medical, Inc. | 31,867 | 97% |
| Tracoe Medical Gmbh | 478 | 1% |
| Teleflex Incorporated | 272 | 1% |
| Premier Dental Products Company | 76 | 0% |
| Sklar Corporation | 70 | 0% |
| Atos Medical Ab | 65 | 0% |
| Technical Products Inc | 60 | 0% |
| Integra Lifesciences Production Corporation | 27 | 0% |
| Ambler Surgical Corp. | 24 | 0% |
| Boston Medical Products, Inc. | 6 | 0% |
| Bausch & Lomb Incorporated | 2 | 0% |
| Surgical Direct, Inc. | 2 | 0% |
Company = labeler of record on GUDID. 14 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 |
|---|---|---|
| JOH | Tube tracheostomy and tube cuff | 35,194 |
| BTO | Tube, tracheostomy (w/wo connector) | 838 |
| BTO | Tube, Tracheostomy (W/Wo Connector) | 610 |
| JOH | Tube Tracheostomy And Tube Cuff | 525 |
| BTR | Tube, Tracheal (W/Wo Connector) | 525 |
| KAC | Tube, Laryngectomy | 65 |
Use these as the dimensions to specify in a tender line.
32,951 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Tracheostomy tube, non-reinforced, non-customized, reusable", from 14 companies. The largest labeler is Icu Medical, Inc. with 97% of records.
JOH (Tube tracheostomy and tube cuff), BTO (Tube, tracheostomy (w/wo connector)), BTO (Tube, Tracheostomy (W/Wo Connector)), JOH (Tube Tracheostomy And Tube Cuff)
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.