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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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MEIKO TopLine Type M2 — 4 UDI-DI variants, MDR

MD Atlas
MEIKO Maschinenbau GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

MEIKO TopLine Type M2

405018700324

4 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: MEIKO Maschinenbau GmbH & Co. KG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 405018700324
Device name: MEIKO TopLine Type M2
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 14, 2025

Manufacturer & authorised representative

Manufacturer

Name: MEIKO Maschinenbau GmbH & Co. KG
SRN: DE-MF-000005536
Country: Germany
Email: info@meiko-global.com
Phone: +49 781 203 0

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KA0N30WVN4KEG8E442RHBM4D

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

-04050187000757
-04050187000764
-04050187000771
-04050187000788