Perfusion Cannula (UDI PCAN3)
Manufactured by INSTITUT GEORGES LOPEZ
Device Regulatory Overview
The Perfusion Cannula (Model/Catalog Number: PCAN3) is a medical device manufactured by INSTITUT GEORGES LOPEZ. This product is indexed under FDA Product Code / Category Classification KDN within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- PCAN3
- Product Code / EMDN
- KDN
- Device Name
- The Cannulation Set provide a connection between an explanted organ and an Organ Perfusion System. Particular compatibility is claimed with the Organ Perfusion System RM4.
- Database Sync Date
- 2026-08-09 09:48:33
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 Perfusion Cannula?
The registered manufacturer of record for Perfusion Cannula is INSTITUT GEORGES LOPEZ.
What is the Primary UDI-DI identifier for Perfusion Cannula?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PCAN3.
What classification code is assigned to this device?
This device is registered under product classification code KDN.
Similar Classification Devices (KDN)
Other Devices by INSTITUT GEORGES LOPEZ
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