GUDIDData
eudamed_udi Primary ID: 07022756044285

Norgesplaster Robust plaster 10 x 10 cm x 6 cm (UDI 07022756044285)

Manufactured by Orkla Wound Care AB

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Norgesplaster Robust plaster 10 x 10 cm x 6 cm - Primary ID 07022756044285

Device Regulatory Overview

The Norgesplaster Robust plaster 10 x 10 cm x 6 cm (Model/Catalog Number: 451143001) is a medical device manufactured by Orkla Wound Care AB. This product is indexed under FDA Product Code / Category Classification M04010199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
451143001
Product Code / EMDN
M04010199
Device Name
TD 04
Database Sync Date
2026-08-09 16:28:52

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 Norgesplaster Robust plaster 10 x 10 cm x 6 cm?

The registered manufacturer of record for Norgesplaster Robust plaster 10 x 10 cm x 6 cm is Orkla Wound Care AB.

What is the Primary UDI-DI identifier for Norgesplaster Robust plaster 10 x 10 cm x 6 cm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07022756044285.

What classification code is assigned to this device?

This device is registered under product classification code M04010199.

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