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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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Lagerungshilfen — 7 UDI-DI variants, MDR (ekamed GmbH & Co. KG)

MD Atlas
ekamed GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Lagerungshilfen

42504181lagZJ

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: ekamed GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42504181lagZJ
Device name: Lagerungshilfen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 31, 2024

Manufacturer & authorised representative

Manufacturer

Name: ekamed GmbH & Co. KG
SRN: DE-MF-000007201
Country: Germany
Email: info@ekamed.de
Phone: +49 5031704100

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01J43SR4ZN4M7KP6K7YJAGMYYT

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

425041811216104250418112161
0425041811215404250418112154
425041811212304250418112123
0425041811217804250418112178
0425041811213004250418112130
0425041811214704250418112147
0425041811211604250418112116