GUDIDData
gudid Primary ID: DP35-0943-201

2.4mm PerCryo Cryoprobe (UDI DP35-0943-201)

Manufactured by Varian Medical Systems, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 2.4mm PerCryo Cryoprobe - Primary ID DP35-0943-201

Device Regulatory Overview

The 2.4mm PerCryo Cryoprobe (Model/Catalog Number: DP35-0943-201) is a medical device manufactured by Varian Medical Systems, Inc.. This product is indexed under FDA Product Code / Category Classification GEH 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.

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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...

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Technical Specifications

Model Number
DP35-0943-201
Product Code / EMDN
GEH
Device Name
Right angle 2.4mm cryoprobe, oblong ice, for use with Cryocare systems
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 2.4mm PerCryo Cryoprobe?

The registered manufacturer of record for 2.4mm PerCryo Cryoprobe is Varian Medical Systems, Inc..

What is the Primary UDI-DI identifier for 2.4mm PerCryo Cryoprobe?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DP35-0943-201.

What classification code is assigned to this device?

This device is registered under product classification code GEH.

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