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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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Extension system — 10 UDI-DI variants, MDR (MARO - Mader, s.r.o.)

MD Atlas
MARO - Mader, s.r.o.

Data from EUDAMED, last updated May 23, 2026

Extension system

859420134E24094

10 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: MARO - Mader, s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 859420134E24094
Device name: Extension system
Device model: EXT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: MARO - Mader, s.r.o.
SRN: CZ-MF-000047386
Country: Czechia
Email: maro@marocz.eu

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01KRB7PYCJVYS319716Y9HGXK0

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

24000908594201340062
24006008594201340093
24001708594201340031
24003608594201340048
24002008594201340024
24002208594201340086
24002508594201340109
24002308594201340017
24001008594201340079
24006208594201340055