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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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Destix MA61 — 10 UDI-DI variants, MDR (ITW LLC & Co. KG)

MD Atlas
ITW LLC & Co. KG

Data from EUDAMED, last updated May 23, 2026

Destix MA61

401911400MAK4

10 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: ITW LLC & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 401911400MAK4
Device name: Destix MA61
Device model: cleaning and disinfection product
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: ITW LLC & Co. KG
SRN: DE-MF-000006443
Country: Germany
Email: mreich@itwindustrialsolutions.com
Phone: +49(0)8006273002

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01KE7BD7PDG6YRSEMA13VQ7PMX

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

DX310004019114000116
DX211204019114090087
DX311004019114000147
DX111204019114000017
DX111404019114000055
DX3110S04019114000154
DX312004019114000178
DX211404019114000109
12031804019114010085
12031604019114010061