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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-60 — 4 UDI-DI variants, MDR

MD Atlas
bon Optic Vertriebsgesellschaft mbH

Data from EUDAMED, last updated May 23, 2026

Refraktionseinheit E-60

426069951e60bonLW

4 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: 426069951e60bonLW
Device name: Refraktionseinheit E-60
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

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JQV3GHFXTF1AM1QZ1755RZ7F

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-6004260699510259
refraction unit E-6004260699510280
refraction unit E-6004260699510273
Refraction unit E-6004260699510266