A device designed for the extracorporeal diffusion of oxygen into blood across a gas-permeable membrane during a cardiopulmonary bypass or extracorporeal membrane oxygenation procedure. It includes a membrane that separates a thin layer of blood from the oxyge
| Company | Devices | Share |
|---|---|---|
| Medtronic, Inc. | 39 | 21% |
| Sorin Group Italia Srl | 35 | 19% |
| Terumo Corporation | 33 | 18% |
| Terumo Cardiovascular Systems Corporation | 28 | 15% |
| Spectrum Medical Srl | 21 | 12% |
| Michigan Critical Care Consultants, Inc. | 11 | 6% |
| Eurosets Srl | 6 | 3% |
| Maquet Cardiopulmonary Ag | 4 | 2% |
| Lifemotion Medical Technology Co., Ltd. | 2 | 1% |
| Breethe, Inc. | 2 | 1% |
| Chalice Medical Limited | 1 | 1% |
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 |
|---|---|---|
| DTZ | OXYGENATOR, CARDIOPULMONARY BYPASS | 124 |
| DTZ | Oxygenator, Cardiopulmonary Bypass | 104 |
| DTR | Heat-Exchanger, Cardiopulmonary Bypass | 36 |
| DTR | HEAT-EXCHANGER, CARDIOPULMONARY BYPASS | 35 |
| DTN | Reservoir, Blood, Cardiopulmonary Bypass | 28 |
| DTM | Filter, blood, cardiopulmonary bypass, arterial line | 23 |
Use these as the dimensions to specify in a tender line.
182 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Extracorporeal membrane oxygenator", from 11 companies. The largest labeler is Medtronic, Inc. with 21% of records.
DTZ (OXYGENATOR, CARDIOPULMONARY BYPASS), DTZ (Oxygenator, Cardiopulmonary Bypass), DTR (Heat-Exchanger, Cardiopulmonary Bypass), DTR (HEAT-EXCHANGER, CARDIOPULMONARY BYPASS)
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.