Saudi Arabia SFDA registration ME0000000256SFDAA00757
DLP® Aortic Root Cannula with Vent Line
Saudi Arabia·Medical Device·Medtronic, Inc.·Class IIIActiveProduct information
Coated Aortic Root Cannula
Product use
This cannula is intended for use during cardiopulmonary bypass for delivering cardioplegia solutions and venting of
the left heart for up to 6 hours. The cannula may be used to aspirate air from the aorta at the conclusion of the bypass
procedure. The Model 24009 cannula may also be used to monitor pressure in the aorta.
Device classification
- Risk Class
- Class III
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000000256SFDAA00757
- Authorization ID
- GHTF-2018-1835
- Status
- Active
- Expire Date
- September 15, 2023
Manufacturer
- Manufacturer Name
- Medtronic, Inc.
Model information
- Model ID(s)
- CB20012
Product accessories
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About this record
Access comprehensive regulatory information for DLP® Aortic Root Cannula with Vent Line in the Saudi Arabia medical device market through Pure Global AI's free database. This Class III device is registered with Saudi Arabia SFDA under registration number ME0000000256SFDAA00757 and manufactured by Medtronic, Inc..
This page provides complete registration details including product category (Medical Device), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.
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