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.

Adhesive specimen microscopy slide (IVD) — 59 UDI-DI variants, IVDR

MD Atlas
Paul Marienfeld GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Adhesive specimen microscopy slide (IVD)

4250317304OTHBU4

59 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: 4250317304OTHBU4
Device name: Adhesive 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: Dec 7, 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

59 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

basicUdiUlid01GKNXDT24520A656EBKH9S271

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

081162104064279010500
081170104250317361349
081160104250317359612
081083104250317361318
081053104250317350169
081081104250317361295
081051104250317350978
081082104250317361301
081052104250317350985
081085104250317361332
081055104250317351005
081084104250317361325
081054104250317350992
081080104250317350916
081050104250317349859
08108019104250317355829
081061804250317351845
080000104250317301871
080000004250317301864
081900009404250317349286
08000919604064279019084
0810002404250317319968
083000104250317353672
083000004250317352088
081000104250317301895

1 2 3