GUDIDData
eudamed_udi Primary ID: 04005800359002

Hansaplast Corn removal plaster with salicylic acid (UDI 04005800359002)

Manufactured by LANGSTEINER SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hansaplast Corn removal plaster with salicylic acid - Primary ID 04005800359002

Device Regulatory Overview

The Hansaplast Corn removal plaster with salicylic acid (Model/Catalog Number: 48841) is a medical device manufactured by LANGSTEINER SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ. This product is indexed under FDA Product Code / Category Classification M0412 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
48841
Product Code / EMDN
M0412
Device Name
Plastry na odciski z kwasem salicylowym
Database Sync Date
2026-08-09 16:48:01

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 Hansaplast Corn removal plaster with salicylic acid?

The registered manufacturer of record for Hansaplast Corn removal plaster with salicylic acid is LANGSTEINER SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ.

What is the Primary UDI-DI identifier for Hansaplast Corn removal plaster with salicylic acid?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04005800359002.

What classification code is assigned to this device?

This device is registered under product classification code M0412.

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