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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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Siodełka prysznicowe — 4 UDI-DI variants, MDR

MD Atlas
INNOW Spółka z ograniczoną odpowiedzialnością Spółka komandytowa

Data from EUDAMED, last updated May 30, 2026

Siodełka prysznicowe

590581741SIODELKAPRYSZSH

4 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: INNOW Spółka z ograniczoną odpowiedzialnością Spółka komandytowa

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 590581741SIODELKAPRYSZSH
Device name: Siodełka prysznicowe
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 13, 2024

Manufacturer & authorised representative

Manufacturer

Name: INNOW Spółka z ograniczoną odpowiedzialnością Spółka komandytowa
SRN: PL-MF-000032529
Country: Poland
Email: marketing2@innow.pl

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01HPGKE4EC5DXJ995B1BC0GNAC

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

C223 EVO05905817412020
C223A EVO05905817412037
C223A05905817411993
C22305905817411986