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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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Medical cabinet — 9 UDI-DI variants, MDR (TORUSCARE Sp. z o.o.)

MD Atlas
TORUSCARE Sp. z o.o.

Data from EUDAMED, last updated May 31, 2026

Medical cabinet

590218602MEDCAB6Y

9 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: TORUSCARE Sp. z o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 590218602MEDCAB6Y
Device name: —
Device model: Medical cabinet
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 13, 2025

Manufacturer & authorised representative

Manufacturer

Name: TORUSCARE Sp. z o.o.
SRN: PL-MF-000047801
Country: Poland
Email: karolina@toruscare.com

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01K2H0HNDFVA506C67WKHKR941

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

SOFERY 105902186021099
SOFERY 205902186021105
SOFERY 305902186021112
SOFERY 405902186021129
SOFERY 505902186021136
SOFERY 605902186021143
SOFERY 705902186021150
SOFERY 805902186021167
SOFERY 905902186021174