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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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EVE! — 27 UDI-DI variants, MDR (BEKA-Hospitec GmbH)

MD Atlas
BEKA-Hospitec GmbH

Data from EUDAMED, last updated May 23, 2026

EVE!

426068189121BP

27 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: BEKA-Hospitec GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426068189121BP
Device name: EVE!
Device model: K121 BEKA Dusch- und Badelifter und deren Zubehöre
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 10, 2024

Manufacturer & authorised representative

Manufacturer

Name: BEKA-Hospitec GmbH
SRN: DE-MF-000013895
Country: Germany
Email: qm@beka-hospitec.de
Phone: +496419222025

Variants by status

UDI-DI variants

27 UDI-DI variants

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Applied filters

basicUdiUlid01HV361E1NBA9HD9MXST99Q3H9

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

K121 BEKA Dusch- und Badelifter und deren Zubehöre04260735020117
K121 BEKA Dusch- und Badelifter und deren Zubehöre04260735020049

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