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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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MANO EDU XL — 8 UDI-DI variants, MDR (Reinecker Vision GmbH)

MD Atlas
Reinecker Vision GmbH

Data from EUDAMED, last updated May 23, 2026

MANO EDU XL

42556338TRABLSR8

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: 42556338TRABLSR8
Device name: MANO EDU XL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2026

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

basicUdiUlid01HHYB1VK17BPP53379YQSSN58

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

MANO120104255633800237
MANO120204255633800244
MANO160104255633800558
MANOEDU104255633800251
MANEDLI104255633800534
MANOPRO104255633800633
MANXXLP304255633800220
MANXXLP204255633800213