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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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Classic — 10 UDI-DI variants, MDR

MD Atlas
ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft

Data from EUDAMED, last updated May 23, 2026

Classic

42502961570LX

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: 42502961570LX
Device name: Classic
Device model: Classic
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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Applied filters

basicUdiUlid01K6A5ZF2B1HB4QGFXXP1K33TT

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

570.00005.759004250296148702
570.00085.759004250296183321
570.00081.759004250296183291
570.00045.759004250296156424
570.00055.759004250296148696
570.00020.759004250296148726
570.00083.759004250296183307
570.00000.759004250296148269
570.00060.759004250296149334
570.00084.759004250296183314