gudid Primary ID: 30052-13

Meso Wound Matrix (UDI 30052-13)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Meso Wound Matrix (Model/Catalog Number: 30052-13) is a medical device manufactured by DSM BIOMEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification KGN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 30052-13
Product Code / EMDN: KGN
Device Name
Database Sync Date: 2026-08-09 09:14:43

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 Meso Wound Matrix?

The registered manufacturer of record for Meso Wound Matrix is DSM BIOMEDICAL, INC..

What is the Primary UDI-DI identifier for Meso Wound Matrix?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 30052-13.

What classification code is assigned to this device?

This device is registered under product classification code KGN.

Similar Classification Devices (KGN)

Other Devices by DSM BIOMEDICAL, INC.

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