Edwards Lifesciences EZ Glide Aortic Cannula (UDI EZC24A)
Manufactured by Edwards Lifesciences LLC
Device Regulatory Overview
The Edwards Lifesciences EZ Glide Aortic Cannula (Model/Catalog Number: EZC24A) is a medical device manufactured by Edwards Lifesciences LLC. This product is indexed under FDA Product Code / Category Classification DWF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EZC24A
- Product Code / EMDN
- DWF
- Device Name
- EZ GLIDE Aortic Cannula
- Database Sync Date
- 2026-08-09 09:04:21
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Edwards Lifesciences EZ Glide Aortic Cannula?
The registered manufacturer of record for Edwards Lifesciences EZ Glide Aortic Cannula is Edwards Lifesciences LLC.
What is the Primary UDI-DI identifier for Edwards Lifesciences EZ Glide Aortic Cannula?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EZC24A.
What classification code is assigned to this device?
This device is registered under product classification code DWF.
Similar Classification Devices (DWF)
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