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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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Armarios accesorios para almacenaje… — 9 UDI-DI variants, MDR

MD Atlas
MOBI-ENDOS,S.L.

Data from EUDAMED, last updated May 23, 2026

Armarios accesorios para almacenaje temporal de fibroscopios y endoscopios

84370243371ARMXA

9 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: MOBI-ENDOS,S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84370243371ARMXA
Device name: Armarios accesorios para almacenaje temporal de fibroscopios y endoscopios
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 14, 2026

Manufacturer & authorised representative

Manufacturer

Name: MOBI-ENDOS,S.L.
SRN: ES-MF-000021771
Country: Spain
Email: administracion@mobi-endos.com
Phone: +34 686589823

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01KEZ9TEH6J9RE7PZXCAK6KNXV

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

ARM4c08437024337607
ARM4fb08437024337577
ARM6c08437024337614
ARM6fb08437024337584
ARM8c08437024337621
ARM8fb08437024337591
ARMIR4c08437024337669
ARMIR6c08437024337676
ARMIR8c08437024337683