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eudamed_udi Primary ID: 04029839420298

FEMUR Komponente UC zementiert (UDI 04029839420298)

Manufactured by Peter Brehm GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FEMUR Komponente UC zementiert - Primary ID 04029839420298

Device Regulatory Overview

The FEMUR Komponente UC zementiert (Model/Catalog Number: 42405-01) is a medical device manufactured by Peter Brehm GmbH. This product is indexed under FDA Product Code / Category Classification P0909030101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
42405-01
Product Code / EMDN
P0909030101
Device Name
FEMUR Komponente UC zementiert
Database Sync Date
2026-08-09 16:29:45

Full Regulatory Attributes

🔒 Token Gated 
{
    "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 FEMUR Komponente UC zementiert?

The registered manufacturer of record for FEMUR Komponente UC zementiert is Peter Brehm GmbH.

What is the Primary UDI-DI identifier for FEMUR Komponente UC zementiert?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04029839420298.

What classification code is assigned to this device?

This device is registered under product classification code P0909030101.

Similar Classification Devices (P0909030101)

Other Devices by Peter Brehm GmbH

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