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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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Rettungstuch / Evakuierungstuch — 4 UDI-DI variants, MDR

MD Atlas
indoor-gruppe

Data from EUDAMED, last updated May 23, 2026

Rettungstuch / Evakuierungstuch

426254356EvaRett00122

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: indoor-gruppe

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426254356EvaRett00122
Device name: Rettungstuch / Evakuierungstuch
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: indoor-gruppe
SRN: DE-MF-000047869
Country: Germany
Email: info@indoor-gruppe.de
Phone: +49 (0371) 6946692

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRXVMBXZ6SGDVYHE0ZE5P0BB

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

093003104262543561615
093004104262543560014
093004504262543560021
093003204262543560007