eudamed_udi Primary ID: 04250108345022

Actosed Plus 2 L (UDI 04250108345022)

Manufactured by ACTO GmbH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Actosed Plus 2 L (Model/Catalog Number: 01.4502.2) is a medical device manufactured by ACTO GmbH. This product is indexed under FDA Product Code / Category Classification D0901 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 01.4502.2
Product Code / EMDN: D0901
Device Name: Invasive Medical Device Disinfectant
Database Sync Date: 2026-08-09 16:49:09

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 Actosed Plus 2 L?

The registered manufacturer of record for Actosed Plus 2 L is ACTO GmbH.

What is the Primary UDI-DI identifier for Actosed Plus 2 L?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250108345022.

What classification code is assigned to this device?

This device is registered under product classification code D0901.

Similar Classification Devices (D0901)

Other Devices by ACTO GmbH

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