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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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MyGeneration — 16,674 UDI-DI variants, MDR

MD Atlas
Schein Orthopädie Service KG

Data from EUDAMED, last updated May 23, 2026

MyGeneration

4055107MyGen69

16,674 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: Schein Orthopädie Service KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4055107MyGen69
Device name: MyGeneration
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: Schein Orthopädie Service KG
SRN: DE-MF-000004958
Country: Germany
Email: remscheid@schein.de
Phone: +4921919100

Variants by status

UDI-DI variants

16,674 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRDT6V93EG5M6DVETC7STS0D

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

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374175000003004048145947886
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379201000002504059465081525
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