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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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RoboFIX — 2 UDI-DI variants, MDR (AKTORmed GmbH)

MD Atlas
AKTORmed GmbH

Data from EUDAMED, last updated May 23, 2026

RoboFIX

42604638400899

2 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: AKTORmed GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42604638400899
Device name: RoboFIX
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 2, 2025

Manufacturer & authorised representative

Manufacturer

Name: AKTORmed GmbH
SRN: DE-MF-000006136
Country: Germany
Email: info@aktormed.com
Phone: +49 9401 93 20 110

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K44VDFDJVCPPS4A3X6FNWCQR

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

24279104260463847918
24279404260463847949