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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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Breathing Circuit Tube & Hose Holder — 4 UDI-DI variants, MDR

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

Data from EUDAMED, last updated May 23, 2026

Breathing Circuit Tube & Hose Holder

859420134DTH250AL

4 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: 859420134DTH250AL
Device name: Breathing Circuit Tube & Hose Holder
Device model: DTH
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 12, 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

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRDNHRJ5D3MT3XEX6GV92243

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

25012208594201340222
25012608594201340215
250122N08594201340246
250126N08594201340239