eudamed_udi Primary ID: 04049852207690

Modular Acetabular Metal Inlay (UDI 04049852207690)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Modular Acetabular Metal Inlay (Model/Catalog Number: 022-2133-2936) is a medical device manufactured by Biotech GmbH. This product is indexed under FDA Product Code / Category Classification P0908030403 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 022-2133-2936
Product Code / EMDN: P0908030403
Device Name: Biotech Acetabular Cup System
Database Sync Date: 2026-08-09 16:28:51

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 Modular Acetabular Metal Inlay?

The registered manufacturer of record for Modular Acetabular Metal Inlay is Biotech GmbH.

What is the Primary UDI-DI identifier for Modular Acetabular Metal Inlay?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04049852207690.

What classification code is assigned to this device?

This device is registered under product classification code P0908030403.

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