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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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GK-20P — 2 UDI-DI variants, IVDR

MD Atlas
MVZ Medizinische Labore Dessau Kassel GmbH

Data from EUDAMED, last updated May 23, 2026

GK-20P

426240865GK20P2K

2 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: MVZ Medizinische Labore Dessau Kassel GmbH

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 426240865GK20P2K
Device name: GK-20P
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Mar 10, 2026

Manufacturer & authorised representative

Manufacturer

Name: MVZ Medizinische Labore Dessau Kassel GmbH
SRN: DE-MF-000033982
Country: Germany
Email: info@laborpraxis-dessau.de
Phone: +49340540530

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KKBX3PMKQ5XH51J45FDR61WB

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

GK-20P-DE04262408650041
GK20P-EN04262408650058