eudamed_udi Primary ID: D-07311410943751DN

Unspecified Brand (UDI D-07311410943751DN)

Manufactured by AKLA AB

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: 94375) is a medical device manufactured by AKLA AB. This product is indexed under FDA Product Code / Category Classification M04040501 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 94375
Product Code / EMDN: M04040501
Device Name: Burngel Dressing
Database Sync Date: 2026-08-09 16:47:08

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is AKLA AB.

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-07311410943751DN.

What classification code is assigned to this device?

This device is registered under product classification code M04040501.

Similar Classification Devices (M04040501)

Other Devices by AKLA AB

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