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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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Moorkissen — 4 UDI-DI variants, MDR (blue bell cosmetic GmbH)

MD Atlas
blue bell cosmetic GmbH

Data from EUDAMED, last updated May 23, 2026

Moorkissen

42502657Bell301YY

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: blue bell cosmetic GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42502657Bell301YY
Device name: Moorkissen
Device model: Wärmekissen, Nackenkissen, Rückenkissen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 9, 2021

Manufacturer & authorised representative

Manufacturer

Name: blue bell cosmetic GmbH
SRN: DE-MF-000005156
Country: Germany
Email: info@blue-bell.de
Phone: +49 2824 20830

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FM1YN26DNRXBCNM6XPERCMHB

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

1526890300404250265701488
1025230121804250265701402
1025230121904250265701419
1025230122004250265701396