A sterile, single lumen, tubular device designed to deliver cardioplegic solution to the aortic root to stop the beating of the heart and maintain it dormant; it may also be used to vent the aorta and the left heart during a cardiopulmonary bypass procedure. I
| Company | Devices | Share |
|---|---|---|
| Med Michigan Holdings, Llc | 49 | 36% |
| Medtronic, Inc. | 33 | 24% |
| Livanova Usa, Inc. | 28 | 20% |
| Sorin Group Italia Srl | 24 | 18% |
| Novosci Corp. | 2 | 1% |
| Microtek Medical Llc | 1 | 1% |
Company = labeler of record on GUDID. 6 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 | 80 |
| DWF | Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypa | 52 |
| DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypa | 20 |
| KKX | Drape, surgical | 1 |
Use these as the dimensions to specify in a tender line.
137 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Cardioplegia cannula", from 6 companies. The largest labeler is Med Michigan Holdings, Llc with 36% 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), KKX (Drape, surgical)
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.
Add cardioplegia cannula to the RFQ basket or use the form below with quantity, specification and delivery location; the Network returns comparable quotes from verified suppliers in 2–5 working days.
Hospitals, pharmacies and distributors anywhere: tell us what you need and the Consulting Wallah Network returns comparable quotes from verified suppliers. No fee for buyers.
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.