GUDIDData
Bulk Audit Tool API Access
enforcement Primary ID: Z-2530-2019

Vanguard XP Tibial Tray 67 mm Item # 195247 (UDI Z-2530-2019)

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 67 mm Item # 195247 - Primary ID Z-2530-2019

Device Regulatory Overview

The Vanguard XP Tibial Tray 67 mm Item # 195247 (Model/Catalog Number: Unspecified) is a medical device manufactured by Zimmer Biomet, Inc.. This product is indexed under FDA Product Code / Category Classification Lot Number 332640 833160 514940 372960 372970 514920 752020 752030 919210 764330 754460 884550 837740 764340 861170 884360 887950 935780 935800 953910 968990 953950 928850 936190 953930 953940 861160 663120 660390 663080 663110 584200 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 →

FARASTAR Ablation Generator EU, Pulsed Field Ablation Generator, Product ID 61M401; Percutaneous Cardiac Ablation Catheter...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2755-2026 View Full Alert →

FARADRIVE STEERABLE SHEATH CLEAR, used to facilitate access to the vasculature and into the chambers of the heart, Material Number 21M402, I...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2793-2026 View Full Alert →

SafeOp Patient Interface, REF: AIX11240, part of SafeOp 3: Neural Informatix System...

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

Technical Specifications

Model Number
N/A
Device Name
Vanguard XP Tibial Tray 67 mm Item # 195247
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
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Vanguard XP Tibial Tray 67 mm Item # 195247?

The registered manufacturer of record for Vanguard XP Tibial Tray 67 mm Item # 195247 is Zimmer Biomet, Inc..

What is the Primary UDI-DI identifier for Vanguard XP Tibial Tray 67 mm Item # 195247?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z-2530-2019.

What classification code is assigned to this device?

This device is registered under product classification code Lot Number 332640 833160 514940 372960 372970 514920 752020 752030 919210 764330 754460 884550 837740 764340 861170 884360 887950 935780 935800 953910 968990 953950 928850 936190 953930 953940 861160 663120 660390 663080 663110 584200.

Other Devices by Zimmer Biomet, Inc.

Programmatic Export

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

JSON API Endpoint