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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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Erkaphon Duo — 10 UDI-DI variants, MDR

MD Atlas
ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft

Data from EUDAMED, last updated May 23, 2026

Erkaphon Duo

42502961541LQ

10 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: ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42502961541LQ
Device name: Erkaphon Duo
Device model: Erkaphon Duo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft
SRN: DE-MF-000009663
Country: Germany
Email: service@erka.org
Phone: +49 (0) 8041/80090

Variants by status

UDI-DI variants

10 UDI-DI variants

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basicUdiUlid01K6A7Z98KF7V5ARG7E9Z5H3ZF

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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

541.00025.759004250296150590
541.00055.759004250296156134
541.00060.759004250296129244
541.00005.759004250296150606
541.00000.759004250296129138
541.00020.759004250296129190
541.00051.759004250296156141
541.00010.759004250296129169
541.00080.759004250296150613
541.00035.759004250296150583