A device consisting of a hollow rubber or rubber-like structure, expandable with either liquid or air, intended to be used to control nose bleeding (epistaxis) of the anterior or posterior nasal cavity. It is applied during an ear/nose/throat (ENT) interventio
| Company | Devices | Share |
|---|---|---|
| Acclarent, Inc. | 38 | 44% |
| Smith & Nephew, Inc. | 12 | 14% |
| Summit Medical, Inc. | 11 | 13% |
| Boston Medical Products, Inc. | 6 | 7% |
| Medtronic Xomed, Inc. | 4 | 5% |
| Mar-Med Inc. | 3 | 3% |
| Invotec International, Inc. | 3 | 3% |
| Fortune Medical Instrument Corp. | 3 | 3% |
| Eon Meditech Private Limited | 3 | 3% |
| Teleflex Incorporated | 2 | 2% |
| Deroyal Industries, Inc. | 2 | 2% |
Company = labeler of record on GUDID. 11 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 |
|---|---|---|
| LRC | INSTRUMENT, ENT MANUAL SURGICAL | 38 |
| EMX | Balloon, Epistaxis | 33 |
| EMX | BALLOON, EPISTAXIS | 24 |
Use these as the dimensions to specify in a tender line.
87 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Nasal haemostatic balloon", from 11 companies. The largest labeler is Acclarent, Inc. with 44% of records.
LRC (INSTRUMENT, ENT MANUAL SURGICAL), EMX (Balloon, Epistaxis), EMX (BALLOON, EPISTAXIS)
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.