GUDIDData
gudid Primary ID: 550763

URGOTUL ABSORB BORDER (UDI 550763)

Manufactured by LABORATOIRES URGO

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for URGOTUL ABSORB BORDER - Primary ID 550763

Device Regulatory Overview

The URGOTUL ABSORB BORDER (Model/Catalog Number: 550763) is a medical device manufactured by LABORATOIRES URGO. This product is indexed under FDA Product Code / Category Classification NAD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
550763
Product Code / EMDN
NAD
Device Name
An adhesive lipido-colloid foam dressing with soft-adherent TLC and silicone border.Composed of :- a soft-adherent TLC layer combined with an absorbent polyurethane foam pad and a superabsorbent layer- a vapour permeable waterproof outer film with silicone adhesive on the edges
Database Sync Date
2026-08-09 09:02:40

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 URGOTUL ABSORB BORDER?

The registered manufacturer of record for URGOTUL ABSORB BORDER is LABORATOIRES URGO.

What is the Primary UDI-DI identifier for URGOTUL ABSORB BORDER?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 550763.

What classification code is assigned to this device?

This device is registered under product classification code NAD.

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