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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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Iriscope — 5 UDI-DI variants, MDR (Lys Medical)

MD Atlas
Lys Medical

Data from EUDAMED, last updated May 23, 2026

Iriscope

PP10078IRIS92

5 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: Lys Medical

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: PP10078IRIS92
Device name: Iriscope
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 31, 2023

Manufacturer & authorised representative

Manufacturer

Name: Lys Medical
SRN: BE-MF-000000036
Country: Belgium
Email: info@lysmedical.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G9Q347Z94JKD52DJXYWPS6XB

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

IRIS-13111998976986
IRIS-18111998977552
IRIS-CTRL112002481851
T-Flush - Push-Pull Lock111998975296
T-Flush - Screw Lock111936237840