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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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Elektrody do defibrylacji — 28 UDI-DI variants, MDR

MD Atlas
SORIMEX sp. z o.o.

Data from EUDAMED, last updated May 31, 2026

Elektrody do defibrylacji

59030022252466

28 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: SORIMEX sp. z o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 59030022252466
Device name: Elektrody do defibrylacji
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 20, 2025

Manufacturer & authorised representative

Manufacturer

Name: SORIMEX sp. z o.o.
SRN: PL-MF-000020958
Country: Poland
Email: office@sorimex.pl
Phone: +48 56 657 77 20

Variants by status

UDI-DI variants

28 UDI-DI variants

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Applied filters

basicUdiUlid01K80GW7CBGGN4MV17HNZYPW1S

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

Electrodes for defibrillation05903002216903
Electrodes for defibrillation05903002216156
Electrodes for defibrillation05903002216620

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