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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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Refraktionseinheit E-30 SE — 8 UDI-DI variants, MDR

MD Atlas
bon Optic Vertriebsgesellschaft mbH

Data from EUDAMED, last updated May 23, 2026

Refraktionseinheit E-30 SE

426069951e30bonKV

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: bon Optic Vertriebsgesellschaft mbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426069951e30bonKV
Device name: Refraktionseinheit E-30 SE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 2, 2025

Manufacturer & authorised representative

Manufacturer

Name: bon Optic Vertriebsgesellschaft mbH
SRN: DE-MF-000006083
Country: Germany
Email: call@bon.de
Phone: +49 451-80 900 0

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JQV3GM74887YW3JEMMWN5B0A

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

refraction unit E-30 SE04260699510143
refraction unit E-30 SE04260699510112
refraction unit E-30 SE04260699510082
refraction unit E-30 SE04260699510075
refraction unit E-30 SE04260699510099
refraction unit E-30 SE04260699510136
refraction unit E-30 SE04260699510129
Refraction unit E-30 SE04260699510105