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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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Vorlesesysteme — 3 UDI-DI variants, MDR (Reinecker Vision GmbH)

MD Atlas
Reinecker Vision GmbH

Data from EUDAMED, last updated May 23, 2026

Vorlesesysteme

42556338VLSZ4

3 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: Reinecker Vision GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 42556338VLSZ4
Device name: Vorlesesysteme
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 18, 2023

Manufacturer & authorised representative

Manufacturer

Name: Reinecker Vision GmbH
SRN: DE-MF-000025998
Country: Germany
Email: info@reineckervision.de
Phone: +49625793110

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HHYE9NS9E17WHTNZXK7XYG2F

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

VOXBOP4004255633800343
VOXBOX4004255633800336
VOXBPRO204255633800350