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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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Plasters — 8 UDI-DI variants, MDR (M.Ex.T. Belgium)

MD Atlas
M.Ex.T. Belgium

Data from EUDAMED, last updated May 23, 2026

Plasters

54009380002-PLL2

8 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: M.Ex.T. Belgium

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 54009380002-PLL2
Device name: Plasters
Device model: Plasters
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: M.Ex.T. Belgium
SRN: BE-MF-000022927
Country: Belgium
Email: qc01@mext.be
Phone: +3251263286

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01KMJP1T449SNR4KJ83HYPTR9K

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

Adhesive plaster blue, 0,02x5m05400938000328
Adhesive plaster silk, 0,0125x5m05400938000304
Adhesive plaster silk, 0,0250x5m05400938000311
Cutastrip, 75x6mm, 5x3pc05400938000014
Duoskin blue, 10x8cm05400938000465
Duoskin blue, 10x8cm05400938000823
Duoskin, 10x6cm05400938000410
Duoskin, 10x6cm05400938000236