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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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Klin Antyrefluksowy — 112 UDI-DI variants, MDR

MD Atlas
Polstar Mateusz Ordyszewski

Data from EUDAMED, last updated May 30, 2026

Klin Antyrefluksowy

590826926antyrefluksowyGW

112 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: Polstar Mateusz Ordyszewski

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 590826926antyrefluksowyGW
Device name: Klin Antyrefluksowy
Device model: Klin Antyrefluksowy
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 16, 2024

Manufacturer & authorised representative

Manufacturer

Name: Polstar Mateusz Ordyszewski
SRN: PL-MF-000036129
Country: Poland
Email: kontakt@alica24.pl

Variants by status

UDI-DI variants

112 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J7X8ZJFKGEEA32TKF1020A7S

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

KA1.1305908269261222
Ka2.905908269261383
KA8.1005908269262328
KA8.305908269260911
KA1.505908269261505
KA5.605908269261659
KA3.905908269262021
KA6.305908269260317
KA1.405908269261475
KA9.1305908269262274
KA2.705908269261369
KA1.605908269262205

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