GUDIDData
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enforcement Primary ID: Z-2503-2019

XP- CR Tibial Tray- Interlok 59mm Item # 195268 (UDI Z-2503-2019)

Manufactured by Zimmer Biomet, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for XP- CR Tibial Tray- Interlok 59mm Item # 195268 - Primary ID Z-2503-2019

Device Regulatory Overview

The XP- CR Tibial Tray- Interlok 59mm Item # 195268 (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 004960 262370 130580 004970 130630 130550 130610 130560 130570 004950 130590 279210 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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Technical Specifications

Model Number
N/A
Device Name
XP- CR Tibial Tray- Interlok 59mm Item # 195268
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 XP- CR Tibial Tray- Interlok 59mm Item # 195268?

The registered manufacturer of record for XP- CR Tibial Tray- Interlok 59mm Item # 195268 is Zimmer Biomet, Inc..

What is the Primary UDI-DI identifier for XP- CR Tibial Tray- Interlok 59mm Item # 195268?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z-2503-2019.

What classification code is assigned to this device?

This device is registered under product classification code Lot Number 004960 262370 130580 004970 130630 130550 130610 130560 130570 004950 130590 279210.

Other Devices by Zimmer Biomet, Inc.

Programmatic Export

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