GUDIDData
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enforcement Primary ID: Z-2537-2019

Vanguard XP Tibial Tray 87 mm Item # 195254 (UDI Z-2537-2019)

Manufactured by Zimmer Biomet, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vanguard XP Tibial Tray 87 mm Item # 195254 - Primary ID Z-2537-2019

Device Regulatory Overview

The Vanguard XP Tibial Tray 87 mm Item # 195254 (Model/Catalog Number: Unspecified) is a medical device manufactured by Zimmer Biomet, Inc.. This product is indexed under FDA Product Code / Category Classification None distributed 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-2753-2026 View Full Alert →

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🔒 Compromised Lot & Serial Numbers Locked
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Technical Specifications

Model Number
N/A
Product Code / EMDN
None distributed
Device Name
Vanguard XP Tibial Tray 87 mm Item # 195254
Database Sync Date
2026-08-09 10:06:36

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 Vanguard XP Tibial Tray 87 mm Item # 195254?

The registered manufacturer of record for Vanguard XP Tibial Tray 87 mm Item # 195254 is Zimmer Biomet, Inc..

What is the Primary UDI-DI identifier for Vanguard XP Tibial Tray 87 mm Item # 195254?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z-2537-2019.

What classification code is assigned to this device?

This device is registered under product classification code None distributed.

Other Devices by Zimmer Biomet, Inc.

Programmatic Export

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