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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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General specimen microscopy slide (IVD) — 265 UDI-DI variants, IVDR

MD Atlas
Paul Marienfeld GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

General specimen microscopy slide (IVD)

4250317302OTMSUX

265 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Paul Marienfeld GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4250317302OTMSUX
Device name: General specimen microscopy slide (IVD)
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jun 23, 2022

Manufacturer & authorised representative

Manufacturer

Name: Paul Marienfeld GmbH & Co. KG
SRN: DE-MF-000023724
Country: Germany
Email: info@marienfeld-superior.com
Phone: +49 9343 6272 0

Variants by status

UDI-DI variants

265 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G68H54QWHNXWP911Z5A8P8GW

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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0705038204064279016595
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