GUDIDData
eudamed_udi Primary ID: 07332343300336

Dermosil Medi Wound & eye cleansing spray 50 ml (UDI 07332343300336)

Manufactured by Aurena Laboratories AB

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dermosil Medi Wound & eye cleansing spray 50 ml - Primary ID 07332343300336

Device Regulatory Overview

The Dermosil Medi Wound & eye cleansing spray 50 ml (Model/Catalog Number: 301421) is a medical device manufactured by Aurena Laboratories AB. This product is indexed under FDA Product Code / Category Classification M04040101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
301421
Product Code / EMDN
M04040101
Device Name
Wound and Eye Wash Spray
Database Sync Date
2026-08-09 18:38:32

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 Dermosil Medi Wound & eye cleansing spray 50 ml?

The registered manufacturer of record for Dermosil Medi Wound & eye cleansing spray 50 ml is Aurena Laboratories AB.

What is the Primary UDI-DI identifier for Dermosil Medi Wound & eye cleansing spray 50 ml?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07332343300336.

What classification code is assigned to this device?

This device is registered under product classification code M04040101.

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