GUDIDData
gudid Primary ID: PRGNX-8008-013

KidneyVault Portable Renal Perfusion System (UDI PRGNX-8008-013)

Manufactured by Paragonix Technologies Inc

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KidneyVault Portable Renal Perfusion System - Primary ID PRGNX-8008-013

Device Regulatory Overview

The KidneyVault Portable Renal Perfusion System (Model/Catalog Number: PRGNX-8008-013) is a medical device manufactured by Paragonix Technologies Inc. This product is indexed under FDA Product Code / Category Classification KDN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PRGNX-8008-013
Product Code / EMDN
KDN
Device Name
8mm Straight Cannula
Database Sync Date
2026-08-09 09:37:49

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of KidneyVault Portable Renal Perfusion System?

The registered manufacturer of record for KidneyVault Portable Renal Perfusion System is Paragonix Technologies Inc.

What is the Primary UDI-DI identifier for KidneyVault Portable Renal Perfusion System?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PRGNX-8008-013.

What classification code is assigned to this device?

This device is registered under product classification code KDN.

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