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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Xtrata Transparent Film Dressing… — 3 UDI-DI variants, MDR

MD Atlas
mediset clinical products GmbH

Data from EUDAMED, last updated May 23, 2026

Xtrata Transparent Film Dressing 10cmx10m

426042286XTRTFRH24W8

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: mediset clinical products GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426042286XTRTFRH24W8
Device name: Xtrata Transparent Film Dressing 10cmx10m
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: mediset clinical products GmbH
SRN: DE-MF-000007347
Country: Germany
Email: info@mediset.de
Phone: +49(0)210436832

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KM3496Y85V7VCG7N9299SP6Y

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Xtrata Transparent Film Dressing 10cmx10m04260422861504
Xtrata Transparent Film Dressing 15cmx10m04260422861511
Xtrata Transparent Film Dressing 5cmx10m04260422861498