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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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DPX new non-aqueous mounting medium… — 1 UDI-DI variant, IVDR

MD Atlas
Merck KGaA

Data from EUDAMED, last updated May 31, 2026

DPX new non-aqueous mounting medium for microscopy

4027269100579UL

1 UDI-DI variant

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: Merck KGaA

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 4027269100579UL
Device name: DPX new non-aqueous mounting medium for microscopy
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: Merck KGaA
SRN: DE-MF-000018777
Country: Germany
Email: service@merckgroup.com
Phone: +49 6151720

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01KST2085J194ED79QFWKBCE9V

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

DPX new non-aqueous mounting medium for microscopy04027269296575