A semi-rigid or rigid tube intended to be surgically inserted into the right atrium or large vein to serve as a channel for the extracorporeal transport of deoxygenated blood from a patient during cardiopulmonary bypass and/or extracorporeal membrane oxygenati
| Company | Devices | Share |
|---|---|---|
| Medtronic, Inc. | 347 | 50% |
| Livanova Usa, Inc. | 99 | 14% |
| Edwards Lifesciences Llc | 87 | 13% |
| Enablecv Inc. | 69 | 10% |
| Sorin Group Italia Srl | 59 | 9% |
| Spectrum Medical Srl | 15 | 2% |
| Med Michigan Holdings, Llc | 5 | 1% |
| B. Braun Medical Inc. | 3 | 0% |
| Angiodynamics, Inc. | 3 | 0% |
| Navilyst Medical, Inc. | 2 | 0% |
Company = labeler of record on GUDID. 10 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 |
|---|---|---|
| DWF | CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPA | 576 |
| DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypa | 202 |
| DWF | Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypa | 94 |
| DQY | CATHETER, PERCUTANEOUS | 25 |
| QHW | Single lumen ECMO cannula | 24 |
| DTL | Adaptor, stopcock, manifold, fitting, cardiopulmonary bypass | 11 |
Use these as the dimensions to specify in a tender line.
689 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage", from 10 companies. The largest labeler is Medtronic, Inc. with 50% of records.
DWF (CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPA), DWF (Catheter, cannula and tubing, vascular, cardiopulmonary bypa), DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypa), DQY (CATHETER, PERCUTANEOUS)
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.