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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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RiEye Mk2S — 1 UDI-DI variant, MDR (Rini Ergoteknik AB)

MD Atlas
Rini Ergoteknik AB

Data from EUDAMED, last updated May 30, 2026

RiEye Mk2S

735013656100-00105-0n6Y

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Rini Ergoteknik AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 735013656100-00105-0n6Y
Device name: RiEye Mk2S
Device model: 100-00105-0n
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 13, 2022

Manufacturer & authorised representative

Manufacturer

Name: Rini Ergoteknik AB
SRN: SE-MF-000028740
Country: Sweden
Email: info@rini.se
Phone: +46 8 594 771 70

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01GF84DE8QR50MHWAZJ7VWEB7W

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

100-00105-0n07350136560002