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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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Optical Ergonomic Solutions — 12 UDI-DI variants, MDR (Optergo AB)

MD Atlas
Optergo AB

Data from EUDAMED, last updated May 30, 2026

Optical Ergonomic Solutions

735015282GaliFUPPriSpecZM

12 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: Optergo AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 735015282GaliFUPPriSpecZM
Device name: —
Device model: Optical Ergonomic Solutions
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Optergo AB
SRN: SE-MF-000032762
Country: Sweden
Email: markus@optergo.com
Phone: +46 31 88 77 27

Variants by status

UDI-DI variants

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSHKWYA3G35CRETXPTGWV537

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

1013107350152820296
1013107350152820265
1013107350152820357
1013107350152820333
1013107350152820319
1013107350152820289
1013107350152820340
1013107350152820326
1013107350152820364
1013107350152820371
1013107350152820272
1013107350152820302