eudamed_udi Primary ID: 04049852219563

Revision hip cup (UDI 04049852219563)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Revision hip cup (Model/Catalog Number: 031-2102-0044) 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: 031-2102-0044
Product Code / EMDN: P0908030301
Device Name: Biotech Acetabular Cup System
Database Sync Date: 2026-08-09 16:29:05

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 Revision hip cup?

The registered manufacturer of record for Revision hip cup is Biotech GmbH.

What is the Primary UDI-DI identifier for Revision hip cup?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04049852219563.

What classification code is assigned to this device?

This device is registered under product classification code P0908030301.

Similar Classification Devices (P0908030301)

Other Devices by Biotech GmbH

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