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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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ICARD L Patient monitor — 1 UDI-DI variant, MDD

MD Atlas
Przedsiębiorstwo Elektroniki Profesjonalnej IGEL Jerzy Kowaliński

Data from EUDAMED, last updated May 30, 2026

ICARD L Patient monitor

B-05905090112822

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIb

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: Przedsiębiorstwo Elektroniki Profesjonalnej IGEL Jerzy Kowaliński

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Device characteristics

Active deviceMeasuring function

Legacy certificates

Certificate number: TNP/MDD/0295/4910/2019
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: TUV NORD Polska Sp. z o.o (2274)
Validity: May 25, 2024

Identity & classification

Basic UDI-DI: B-05905090112822
Device name: ICARD L Patient monitor
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: May 19, 2022

Manufacturer & authorised representative

Manufacturer

Name: Przedsiębiorstwo Elektroniki Profesjonalnej IGEL Jerzy Kowaliński
SRN: PL-MF-000022162
Country: Poland
Email: igel@igel.pl
Phone: +48 32 271 76 90

Variants by status

UDI-DI variants

1 UDI-DI variant

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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

ICARD L Patient Monitor05905090112822