GUDIDData
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gudid Primary ID: 3240-31

CORB (UDI 3240-31)

Manufactured by Zimmer, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CORB - Primary ID 3240-31

Device Regulatory Overview

The CORB (Model/Catalog Number: 3240-31) is a medical device manufactured by Zimmer, Inc.. This product is indexed under FDA Product Code / Category Classification HSZ 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-2578-2026 View Full Alert →

Brand Name: Persona Revision Product Name: Persona Revision Trabecular Metal Femoral Distal Augment Model/Catalog Number: 42-5572-066-10 ...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2529-2026 View Full Alert →

Off-Axis Comprehensive Shoulder System, Large, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040242...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2531-2026 View Full Alert →

Off-Axis Alliance Glenoid, Right, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040476...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
3240-31
Product Code / EMDN
HSZ
Device Name
Database Sync Date
2026-08-09 09:19:26

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 CORB?

The registered manufacturer of record for CORB is Zimmer, Inc..

What is the Primary UDI-DI identifier for CORB?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3240-31.

What classification code is assigned to this device?

This device is registered under product classification code HSZ.

Similar Classification Devices (HSZ)

Other Devices by Zimmer, Inc.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

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