Saudi Arabia SFDA registration ME0000000256SFDAA00005
DLP® Aortic Root Cannula
Saudi Arabia·Medical Device·Medtronic, Inc.·Class IIActiveProduct information
Uncoated Standard Aortic Cannulae
Product use
This cannula is intended for short term use (six hours or less) in conjunction with cardiopulmonary bypass surgery
for delivering cardioplegia solutions. The cannula may also be used to aspirate air from the aorta at the conclusion
of the bypass procedure.
The Model 23009 cannula may also be used to monitor pressure in the aorta.
Device classification
- Risk Class
- Class II
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000000256SFDAA00005
- Authorization ID
- MDMA-1-2020-0257
- Status
- Active
- Expire Date
- January 17, 2026
Manufacturer
- Manufacturer Name
- Medtronic, Inc.
Model information
- Model ID(s)
- 10009 10012 10014 10016 10018 10112 10112WF 10114B 10114 10114WF 20009 20012 20012s 20014l 20014 20016 20112B 20112 20114B 20114HWF 20114 20114WF 23009 24009
Product accessories
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About this record
Access comprehensive regulatory information for DLP® Aortic Root Cannula in the Saudi Arabia medical device market through Pure Global AI's free database. This Class II device is registered with Saudi Arabia SFDA under registration number ME0000000256SFDAA00005 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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