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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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ExamVision Loupe System — 4 UDI-DI variants, MDR (ExamVision A/S)

MD Atlas
ExamVision A/S

Data from EUDAMED, last updated May 23, 2026

ExamVision Loupe System

574400023EVLoupeXD

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: ExamVision A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 574400023EVLoupeXD
Device name: ExamVision Loupe System
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 12, 2024

Manufacturer & authorised representative

Manufacturer

Name: ExamVision A/S
SRN: DK-MF-000032397
Country: Denmark
Email: Compliance@ExamVision.com
Phone: +4587921210

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HPEY859WBWTVMXFY54PXXGX2

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

ExamVision Loupe System Kepler Kompakt 3.5x05744000230061
KK3405744000230351
KK5005744000230368
KK7605744000230375