GUDIDData
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gudid Primary ID: IB-CON

IntelliBlate Microwave Ablation System Console (UDI IB-CON)

Manufactured by Varian Medical Systems, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IntelliBlate Microwave Ablation System Console - Primary ID IB-CON

Device Regulatory Overview

The IntelliBlate Microwave Ablation System Console (Model/Catalog Number: IB-CON) is a medical device manufactured by Varian Medical Systems, Inc.. This product is indexed under FDA Product Code / Category Classification NEY within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-0990-2017 View Full Alert →

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ID: Z-0760-2013 View Full Alert →

Rectal Retractors, titanium, item # AL07368000, a component of Varian Medical Ring and Tandem Applicator Sets; Intended for use in Brachyth...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-1324-2013 View Full Alert →

Segmented Cylinder Applicator Set, Model # GM11004150, when used for Pulsed Dose Rate (PDR) Product Usage: Usage: Used during pulsed do...

🔒 Compromised Lot & Serial Numbers Locked
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Technical Specifications

Model Number
IB-CON
Product Code / EMDN
NEY
Device Name
IntelliBlate microwave ablation system console only for tabletop configuration
Database Sync Date
2026-08-09 09:22:18

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 IntelliBlate Microwave Ablation System Console?

The registered manufacturer of record for IntelliBlate Microwave Ablation System Console is Varian Medical Systems, Inc..

What is the Primary UDI-DI identifier for IntelliBlate Microwave Ablation System Console?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is IB-CON.

What classification code is assigned to this device?

This device is registered under product classification code NEY.

Similar Classification Devices (NEY)

Other Devices by Varian Medical Systems, Inc.

Programmatic Export

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