Device Explorer · FDA GUDID · GMDN 36109

Coronary sinus cannula

A sterile, rigid or semi-rigid tube designed to be surgically inserted, temporarily, into the ostium of the coronary sinus to provide retrograde coronary perfusion/cardioplegia during cardiopulmonary bypass or minimally invasive surgery. It may be equipped wit

US‑registered devices160in commercial distribution
Companies7labelers on GUDID
Single‑use89%of device records
Sterile92%labelled sterile
Prescription62%Rx‑only share
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Share of device records

Livanova Usa, Inc.4931%
Medtronic, Inc.4830%
Edwards Lifesciences Llc3019%
Enablecv Inc.138%
Peak Medical Distribution Inc.128%
Teleflex Incorporated53%
Sorin Group Italia Srl32%

Top labelers

CompanyDevicesShare
Livanova Usa, Inc.4931%
Medtronic, Inc.4830%
Edwards Lifesciences Llc3019%
Enablecv Inc.138%
Peak Medical Distribution Inc.128%
Teleflex Incorporated53%
Sorin Group Italia Srl32%

Company = labeler of record on GUDID. 7 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

enableCV Retrograde Cardioplegia CatheterenableCV ProPlege Peripheral Retrograde CardioplCoronary sinus cannulaCoronary artery cannulaCP-xxxxxProPlege Device KitEdwards Lifesciences Retrograde Cardioplegia CatGundry®DLP®PILLINGPEAK MEDICALCoronary Sinus Cannula

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
DWFCATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPA184
DWFCatheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypa13
GEACannula, Surgical, General & Plastic Surgery12
KRACatheter, continuous flush5
DWFCatheter, cannula and tubing, vascular, cardiopulmonary bypa3
GAANeedle, Aspiration And Injection, Disposable1

GMDN & GCC registration

  • GMDN code 36109 · non‑implantable
  • Single‑use 89% · sterile 92% · Rx‑only 62% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Catheter Gauge (French) · 102Length (Centimeter) · 5Width (Inch) · 5

Use these as the dimensions to specify in a tender line.

How many coronary sinus cannula products are registered in the US?

160 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Coronary sinus cannula", from 7 companies. The largest labeler is Livanova Usa, Inc. with 31% of records.

Which FDA product codes apply?

DWF (CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPA), DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypa), GEA (Cannula, Surgical, General & Plastic Surgery), KRA (Catheter, continuous flush)

Is this the same as UAE/GCC registration?

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.

How do I get quotes?

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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.

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