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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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Przedłużka, lina regulowana — 6 UDI-DI variants, MDR

MD Atlas
Si-iS Paweł Wyszyński

Data from EUDAMED, last updated May 31, 2026

Przedłużka, lina regulowana

590709726PRZEDLUZKA7W

6 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: Si-iS Paweł Wyszyński

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 590709726PRZEDLUZKA7W
Device name: Przedłużka, lina regulowana
Device model: Przedłużka, lina regulowana 50 cm
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 20, 2025

Manufacturer & authorised representative

Manufacturer

Name: Si-iS Paweł Wyszyński
SRN: PL-MF-000044189
Country: Poland
Email: sklep@si-is.pl
Phone: +48790208338

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01K33Y2QD5DHNG62WRX8C41723

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

590709726074205907097260742
590709726075905907097260759
590709726076605907097260766
590709726077305907097260773
590709726078005907097260780
590709726073505907097260735