GUDIDData
eudamed_udi Primary ID: 15036631009916

opus stoma care liftplus medical adhesive remover non sting spray (UDI 15036631009916)

Manufactured by Alliance Pharmaceuticals Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for opus stoma care liftplus medical adhesive remover non sting spray - Primary ID 15036631009916

Device Regulatory Overview

The opus stoma care liftplus medical adhesive remover non sting spray (Model/Catalog Number: 5503) is a medical device manufactured by Alliance Pharmaceuticals Limited. This product is indexed under FDA Product Code / Category Classification A108005 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
5503
Product Code / EMDN
A108005
Device Name
Lift Plus Spray
Database Sync Date
2026-08-09 16:29:50

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 opus stoma care liftplus medical adhesive remover non sting spray?

The registered manufacturer of record for opus stoma care liftplus medical adhesive remover non sting spray is Alliance Pharmaceuticals Limited.

What is the Primary UDI-DI identifier for opus stoma care liftplus medical adhesive remover non sting spray?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 15036631009916.

What classification code is assigned to this device?

This device is registered under product classification code A108005.

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