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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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VADOplex — 5 UDI-DI variants, MDR (OPED GmbH)

MD Atlas
OPED GmbH

Data from EUDAMED, last updated May 23, 2026

VADOplex

4046618Z120607VX8H

5 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: OPED GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4046618Z120607VX8H
Device name: VADOplex
Device model: VXSY-10-1
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: OPED GmbH
SRN: DE-MF-000008286
Country: Germany
Email: info@oped.de

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KP37PHD8EPEKEGGS0NKF5FT5

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

VXSY-10-1-PL04046618014660
VXSY-10-104046618014219
VXSY-10-104046618014417
VXSY-10-104046618014561
VXSY-10-104046618014615