GUDIDData
eudamed_udi Primary ID: 05060031475548

Advazorb Border (UDI 05060031475548)

Manufactured by Brightwake Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Advazorb Border - Primary ID 05060031475548

Device Regulatory Overview

The Advazorb Border (Model/Catalog Number: CR4191) is a medical device manufactured by Brightwake Limited. This product is indexed under FDA Product Code / Category Classification M040499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CR4191
Product Code / EMDN
M040499
Device Name
Advazorb Border
Database Sync Date
2026-08-09 16:28:48

Full Regulatory Attributes

πŸ”’ 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 Advazorb Border?

The registered manufacturer of record for Advazorb Border is Brightwake Limited.

What is the Primary UDI-DI identifier for Advazorb Border?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060031475548.

What classification code is assigned to this device?

This device is registered under product classification code M040499.

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