Saudi Arabia SFDA registration ME0000000256SFDAA00752
EOPA® Elongated One-Piece Arterial Cannula
Saudi Arabia·Medical Device·Medtronic, Inc.·Class IIIActiveProduct information
Coated Arterial Cannula
Product use
This product is intended for use with cardiopulmonary bypass as an arterial return cannula for up to 6 hours.
Device classification
- Risk Class
- Class III
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000000256SFDAA00752
- Authorization ID
- GHTF-2018-1835
- Status
- Active
- Expire Date
- September 15, 2023
Manufacturer
- Manufacturer Name
- Medtronic, Inc.
Model information
- Model ID(s)
- CB77420; CB77422; CB77520; CB77522; CB77618; CB77620; CB77622; CB77720; CB77722;
Product accessories
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About this record
Access comprehensive regulatory information for EOPA® Elongated One-Piece Arterial Cannula 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 ME0000000256SFDAA00752 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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