eudamed_udi Primary ID: 04049852297325

Müller Acetabular Cup, Dysplasia (UDI 04049852297325)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Müller Acetabular Cup, Dysplasia (Model/Catalog Number: 021-0505-7026) is a medical device manufactured by Biotech GmbH. This product is indexed under FDA Product Code / Category Classification P090803010102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 021-0505-7026
Product Code / EMDN: P090803010102
Device Name: Biotech Acetabular Cup System
Database Sync Date: 2026-08-09 16:28:57

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, Dysplasia?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04049852297325.

What classification code is assigned to this device?

This device is registered under product classification code P090803010102.

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