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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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EZ-Dop K1 — 3 UDI-DI variants, MDR (Compumedics Germany GmbH)

MD Atlas
Compumedics Germany GmbH

Data from EUDAMED, last updated May 23, 2026

EZ-Dop K1

4260493319000VL

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Compumedics Germany GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4260493319000VL
Device name: EZ-Dop K1
Device model: EZ-Dop Series
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 14, 2026

Manufacturer & authorised representative

Manufacturer

Name: Compumedics Germany GmbH
SRN: DE-MF-000005586
Country: Germany
Email: info@dwl.de
Phone: +49 7731 79 769 0

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRKWNV1C9JDVDX2AN74QFA0K

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

EZ Dop K104260493312554
EZ-Dop04260493312738
EZ-Dop04260493312745