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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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VERDE — 8 UDI-DI variants, MDR (Reinecker Vision GmbH)

MD Atlas
Reinecker Vision GmbH

Data from EUDAMED, last updated May 23, 2026

VERDE

42556338VERDEQ5

8 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: 42556338VERDEQ5
Device name: VERDE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 17, 2025

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

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K7RABG680003NVQ64RB8B28N

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

VERDEAFHD04255633800688
VERMEZ0104255633800695
VERMEZ2004255633800657
VERMEZ2204255633800664
VERMEZ2404255633800671
VERVM20104255633800701
VERVM22104255633800718
VERME22L04255633800725