eudamed_udi
Primary ID: 06009668350285
Cerdak Ceramic Wound Dressing (UDI 06009668350285)
Manufactured by Cerdak (Pty) Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cerdak Ceramic Wound Dressing - Primary ID 06009668350285
Device Regulatory Overview
The Cerdak Ceramic Wound Dressing (Model/Catalog Number: S01015020) is a medical device manufactured by Cerdak (Pty) Ltd. This product is indexed under FDA Product Code / Category Classification M04010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S01015020
- Product Code / EMDN
- M04010101
- Device Name
- Cerdak Drydoc
- Database Sync Date
- 2026-08-09 16:47:03
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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Get API Token Access ($49/mo)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 06009668350285.
What classification code is assigned to this device?
This device is registered under product classification code M04010101.
Similar Classification Devices (M04010101)
Other Devices by Cerdak (Pty) Ltd
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