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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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Medicare-Pool-Lift — 5 UDI-DI variants, MDR (BEKA-Hospitec GmbH)

MD Atlas
BEKA-Hospitec GmbH

Data from EUDAMED, last updated May 23, 2026

Medicare-Pool-Lift

426068189125BX

5 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: 426068189125BX
Device name: Medicare-Pool-Lift
Device model: K125 BEKA Medicare Pool Lifter und deren Zubehör
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

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HV3AW2MMNXJF5XPXW507T31M

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

K125 BEKA Medicare Pool Lifter und deren Zubehör04260681890369
K125 BEKA Medicare Pool Lifter und deren Zubehör04260681890390
K125 BEKA Medicare Pool Lifter und deren Zubehör04260681890383
K125 BEKA Medicare Pool Lifter und deren Zubehör04260681890376
K125 BEKA Medicare Pool Lifter und deren Zubehör04260681890185