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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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Otoskop OX2 — 4 UDI-DI variants, MDR (Orlvision GmbH)

MD Atlas
Orlvision GmbH

Data from EUDAMED, last updated May 23, 2026

Otoskop OX2

426049941OTOLL

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: Orlvision GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426049941OTOLL
Device name: Otoskop OX2
Device model: OX2
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 30, 2022

Manufacturer & authorised representative

Manufacturer

Name: Orlvision GmbH
SRN: DE-MF-000013894
Country: Germany
Email: info@orlvision.de
Phone: +496441 6792990

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01G4A4YZA3R4PP4XPNNVQT4W7W

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

ATMOS Video Otoskop04260499410056
ATMOS Video Otoskop V204260499410230
Otoskop OX204260499410131
M-304-00000-400004260499410223