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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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VARIO Basic — 2 UDI-DI variants, MDR (Meditech Sachsen GmbH)

MD Atlas
Meditech Sachsen GmbH

Data from EUDAMED, last updated May 23, 2026

VARIO Basic

426236658VARIOconstE4

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Meditech Sachsen GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426236658VARIOconstE4
Device name: VARIO Basic
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 29, 2023

Manufacturer & authorised representative

Manufacturer

Name: Meditech Sachsen GmbH
SRN: DE-MF-000026657
Country: Germany
Email: info@meditech-sachsen.de
Phone: +49 35955 746-600

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01GWP4Q70KH9Z7YPXF8CAQEAV8

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

5243304262366580046
8748904262366580053