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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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icebein medical cuffs — 7 UDI-DI variants, MDR (icebein GmbH)

MD Atlas
icebein GmbH

Data from EUDAMED, last updated May 23, 2026

icebein medical cuffs

426250254IBMH20246W

7 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: icebein GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426250254IBMH20246W
Device name: icebein medical cuffs
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: icebein GmbH
SRN: DE-MF-000044945
Country: Germany
Email: info@icebein.com
Phone: +49 (0) 63599170217

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01JC0DC51SEXTFP6SS5KTXQBXV

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

240004262502540163
2100-0604262502540064
2100-0504262502540040
2100-0404262502540057
2300-0204262502540149
2300-0104262502540156
220004262502540132