eudamed_udi Primary ID: 04049852297875

Müller Acetabular Cup for Revision (UDI 04049852297875)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Müller Acetabular Cup for Revision (Model/Catalog Number: 021-1301-6826) is a medical device manufactured by Biotech GmbH. This product is indexed under FDA Product Code / Category Classification P0908030301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 021-1301-6826
Product Code / EMDN: P0908030301
Device Name: Biotech Acetabular Cup System
Database Sync Date: 2026-08-09 16:28:48

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 Müller Acetabular Cup for Revision?

The registered manufacturer of record for Müller Acetabular Cup for Revision is Biotech GmbH.

What is the Primary UDI-DI identifier for Müller Acetabular Cup for Revision?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04049852297875.

What classification code is assigned to this device?

This device is registered under product classification code P0908030301.

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