eudamed_udi Primary ID: D-ZA-MF-000010888AR

Cerdak Ceramic Wound Dressing (UDI D-ZA-MF-000010888AR)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Cerdak Ceramic Wound Dressing (Model/Catalog Number: 600966835) is a medical device manufactured by Cerdak (Pty) Ltd. This product is indexed under FDA Product Code / Category Classification M04010101,M04010102,M040204 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 600966835
Product Code / EMDN: M04010101,M04010102,M040204
Device Name: Cerdak Ceramic Wound Dressing
Database Sync Date: 2026-08-09 17:46:33

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 Cerdak Ceramic Wound Dressing?

The registered manufacturer of record for Cerdak Ceramic Wound Dressing is Cerdak (Pty) Ltd.

What is the Primary UDI-DI identifier for Cerdak Ceramic Wound Dressing?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-ZA-MF-000010888AR.

What classification code is assigned to this device?

This device is registered under product classification code M04010101,M04010102,M040204.

Other Devices by Cerdak (Pty) Ltd

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