GUDIDData
eudamed_udi Primary ID: 05709817517675

Dansac (UDI 05709817517675)

Manufactured by Dansac A/S

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dansac - Primary ID 05709817517675

Device Regulatory Overview

The Dansac (Model/Catalog Number: 1208-43) is a medical device manufactured by Dansac A/S. This product is indexed under FDA Product Code / Category Classification A10020302 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1208-43
Product Code / EMDN
A10020302
Device Name
2-Piece High Output Ostomy Pouch
Database Sync Date
2026-08-09 16:29:47

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 Dansac?

The registered manufacturer of record for Dansac is Dansac A/S.

What is the Primary UDI-DI identifier for Dansac?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05709817517675.

What classification code is assigned to this device?

This device is registered under product classification code A10020302.

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