eudamed_udi Primary ID: 04260735020513

CARLO Alu Classic 185 (UDI 04260735020513)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The CARLO Alu Classic 185 (Model/Catalog Number: K120 BEKA Lifter und deren Zubehör) is a medical device manufactured by BEKA-Hospitec GmbH. This product is indexed under FDA Product Code / Category Classification V0805030102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: K120 BEKA Lifter und deren Zubehör
Product Code / EMDN: V0805030102
Device Name: CARLO Alu Classic 185
Database Sync Date: 2026-08-09 16:46:23

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 CARLO Alu Classic 185?

The registered manufacturer of record for CARLO Alu Classic 185 is BEKA-Hospitec GmbH.

What is the Primary UDI-DI identifier for CARLO Alu Classic 185?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260735020513.

What classification code is assigned to this device?

This device is registered under product classification code V0805030102.

Similar Classification Devices (V0805030102)

Other Devices by BEKA-Hospitec GmbH

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