eudamed_udi Primary ID: 05051659207567

ANCALE PS FEMORAL COMPONENT CEMENTED RIGHT SIZE 1 (UDI 05051659207567)

Manufactured by Covision Medical Technologies Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ANCALE PS FEMORAL COMPONENT CEMENTED RIGHT SIZE 1 (Model/Catalog Number: 02.0228) is a medical device manufactured by Covision Medical Technologies Ltd.. This product is indexed under FDA Product Code / Category Classification P0909030101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 02.0228
Product Code / EMDN: P0909030101
Device Name: ANCALE PS FEMORAL COMPONENT CEMENTED RIGHT SIZE 1
Database Sync Date: 2026-08-09 16:29:26

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 ANCALE PS FEMORAL COMPONENT CEMENTED RIGHT SIZE 1?

The registered manufacturer of record for ANCALE PS FEMORAL COMPONENT CEMENTED RIGHT SIZE 1 is Covision Medical Technologies Ltd..

What is the Primary UDI-DI identifier for ANCALE PS FEMORAL COMPONENT CEMENTED RIGHT SIZE 1?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051659207567.

What classification code is assigned to this device?

This device is registered under product classification code P0909030101.

Similar Classification Devices (P0909030101)

Other Devices by Covision Medical Technologies Ltd.

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