Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

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

121633204250317302601
121703104250317343284
121737104250317360892
121574004250317337306
121654104250317302793
121654304250317302816
121654404250317302823
121654004250317302786
121654204250317302809
121687204250317359681
1216800904250317343031
1216054096904250317331007
121605004250317354549
121722304250317358295
121721304250317358288
121567104250317302496
121567304250317302519
121567404250317302526
121567004250317302489
121567204250317302502
121517104250317348678
121517004064279014041
123517204250317339447
121725004250317359018
121745009104064279013105

2 3 4 5 6