gudid
Primary ID: 415805
Coronary Artery Perfusion Cannula (UDI 415805)
Manufactured by VITALCOR, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Coronary Artery Perfusion Cannula - Primary ID 415805
Device Regulatory Overview
The Coronary Artery Perfusion Cannula (Model/Catalog Number: 415805) is a medical device manufactured by VITALCOR, INC. This product is indexed under FDA Product Code / Category Classification DWF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 415805
- Product Code / EMDN
- DWF
- Device Name
- Coronary Artery Perfusion Cannula with balloon
- Database Sync Date
- 2026-08-09 09:49:36
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 Coronary Artery Perfusion Cannula?
The registered manufacturer of record for Coronary Artery Perfusion Cannula is VITALCOR, INC.
What is the Primary UDI-DI identifier for Coronary Artery Perfusion Cannula?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 415805.
What classification code is assigned to this device?
This device is registered under product classification code DWF.
Similar Classification Devices (DWF)
Other Devices by VITALCOR, INC
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