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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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Kobold — 36 UDI-DI variants, MDR

MD Atlas
ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft

Data from EUDAMED, last updated May 23, 2026

Kobold

42502961223L7

36 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

Measuring function

Identity & classification

Basic UDI-DI: 42502961223L7
Device name: Kobold
Device model: Kobold
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 25, 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

36 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K5ZXS8V5NNRR64XTBAXJ9NS9

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

227.71293.729004250296155373
227.28493.729004250296154567
224.26493.729004250296154086
227.71193.729004250296155410
224.20493.729004250296154093
225.71293.729004250296167147
225.29493.729004250296154895
224.24493.729004250296154109
223.27493.729004250296153881
223.26493.729004250296153898
225.28493.729004250296154406

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