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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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SilentCloud — 4 UDI-DI variants, MDR (Aureliym GmbH)

MD Atlas
Aureliym GmbH

Data from EUDAMED, last updated May 23, 2026

SilentCloud

426076876UTMSL7

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Aureliym GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426076876UTMSL7
Device name: SilentCloud
Device model: SilentCloud
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Jul 20, 2023

Manufacturer & authorised representative

Manufacturer

Name: Aureliym GmbH
SRN: DE-MF-000013571
Country: Germany
Email: info@aureliym.com
Phone: +49 (0) 2641 9082873

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H5SMPMB343P1P6FAR9S2VMTT

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

01004260768760103
02004260768760202
03004260768760301
04004260768760400