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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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MOTOmed layson — 11 UDI-DI variants, MDR (RECK-Technik GmbH & Co. KG)

MD Atlas
RECK-Technik GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

MOTOmed layson

4260193710037R

11 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: RECK-Technik GmbH & Co. KG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4260193710037R
Device name: MOTOmed layson
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: RECK-Technik GmbH & Co. KG
SRN: DE-MF-000005730
Country: Germany
Email: vigilance@motomed.com

Variants by status

UDI-DI variants

11 UDI-DI variants

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Applied filters

basicUdiUlid01KF0AY7PFKFQ2ZXHWV3J75HBB

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

261.21004260193710407
261.60004260193710650
261.11904260193710414
261.31004260193710391
261.13004260193710339
261.33004260193710377
261.11004260193710353
261.13904260193710421
261.01004260193710360
261.03004260193710346
261.23004260193710384