eudamed_udi Primary ID: 04895200304418

Anchor plate (UDI 04895200304418)

Manufactured by Regal Prosthesis Limited

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Anchor plate (Model/Catalog Number: 2-01-4S23-01) is a medical device manufactured by Regal Prosthesis Limited. This product is indexed under FDA Product Code / Category Classification Y062415 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 2-01-4S23-01
Product Code / EMDN: Y062415
Device Name: Prosthetic Knee-joints and Hip-joints
Database Sync Date: 2026-08-09 16:45:06

Full Regulatory Attributes

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{
    "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 Anchor plate?

The registered manufacturer of record for Anchor plate is Regal Prosthesis Limited.

What is the Primary UDI-DI identifier for Anchor plate?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04895200304418.

What classification code is assigned to this device?

This device is registered under product classification code Y062415.

Similar Classification Devices (Y062415)

Other Devices by Regal Prosthesis Limited

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