A sterile flexible tube designed with a balloon at or near the distal tip that may be introduced directly (usually under fluoroscopic guidance) or through a bronchoscope so that its distal tip reaches the bronchi, permitting the inflation of the balloon after
| Company | Devices | Share |
|---|---|---|
| Dongguan Tt Medical, Inc. | 24 | 22% |
| Merit Medical Systems, Inc. | 23 | 21% |
| Acclarent, Inc. | 14 | 13% |
| Disa Medinotec (Pty) Ltd | 10 | 9% |
| Bryan Medical, Inc. | 9 | 8% |
| E.T. View Ltd | 8 | 7% |
| Boston Scientific Corporation | 6 | 6% |
| Fuji Systems Corporation | 4 | 4% |
| Shenzhen Insighters Medical Technology Co., Ltd. | 3 | 3% |
| Teleflex Incorporated | 3 | 3% |
| Pulmonx Corporation | 3 | 3% |
| Fujifilm Corporation | 1 | 1% |
Company = labeler of record on GUDID. 13 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 |
|---|---|---|
| KTI | Bronchoscope Accessory | 34 |
| KTI | BRONCHOSCOPE ACCESSORY | 28 |
| CBI | Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Con | 18 |
| KTI | Bronchoscope accessory | 15 |
| EOQ | Bronchoscope (Flexible Or Rigid) | 11 |
| BTR | Tube, Tracheal (W/Wo Connector) | 6 |
Use these as the dimensions to specify in a tender line.
No closely related category with 50+ devices.
109 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Bronchial balloon catheter", from 13 companies. The largest labeler is Dongguan Tt Medical, Inc. with 22% of records.
KTI (Bronchoscope Accessory), KTI (BRONCHOSCOPE ACCESSORY), CBI (Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Con), KTI (Bronchoscope accessory)
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.