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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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Bildschirmlesesystem — 15 UDI-DI variants, MDR (Reinecker Vision GmbH)

MD Atlas
Reinecker Vision GmbH

Data from EUDAMED, last updated May 23, 2026

Bildschirmlesesystem

42556338BLSVY

15 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: 42556338BLSVY
Device name: Bildschirmlesesystem
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 15, 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

15 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HG8F342TYKQ4ETGNTQY9T3V7

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

MEZZO2K104255633800060
MEZEDU0104255633800053
MEZF20X104255633800015
MEZFO20004255633800046
MEZF24X104255633800039
VEVA243204255633800077
VEVED24204255633800107
VEVED24304255633800114
VEVSP24204255633800091
VEVSW24204255633800084
VEOVOX2404255633800145
VEOVO24104255633800152
VIDEO20104255633800121
VIDEO221F04255633800770
VIDEO24104255633800138