GUDIDData
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eudamed_udi Primary ID: 00810563020717

1.7 mm Round Ice PerCryo™ Cryoprobe (UDI 00810563020717)

Manufactured by Varian Medical Systems, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 1.7 mm Round Ice PerCryo™ Cryoprobe - Primary ID 00810563020717

Device Regulatory Overview

The 1.7 mm Round Ice PerCryo™ Cryoprobe (Model/Catalog Number: DP35-0942-206) is a medical device manufactured by Varian Medical Systems, Inc.. This product is indexed under FDA Product Code / Category Classification Z120102 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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🔒 Compromised Lot & Serial Numbers Locked
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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
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
DP35-0942-206
Product Code / EMDN
Z120102
Device Name
Slimline Cryoprobes
Database Sync Date
2026-08-09 16:58:24

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 1.7 mm Round Ice PerCryo™ Cryoprobe?

The registered manufacturer of record for 1.7 mm Round Ice PerCryo™ Cryoprobe is Varian Medical Systems, Inc..

What is the Primary UDI-DI identifier for 1.7 mm Round Ice PerCryo™ Cryoprobe?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00810563020717.

What classification code is assigned to this device?

This device is registered under product classification code Z120102.

Similar Classification Devices (Z120102)

Other Devices by Varian Medical Systems, Inc.

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