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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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Duszek elastyczny — 6 UDI-DI variants, MDR

MD Atlas
VEST-POL Group Sp. z o.o.

Data from EUDAMED, last updated May 31, 2026

Duszek elastyczny

590515557DUSZEKNA

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: VEST-POL Group Sp. z o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 590515557DUSZEKNA
Device name: Duszek elastyczny
Device model: Duszek elastyczny
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: VEST-POL Group Sp. z o.o.
SRN: PL-MF-000003439
Country: Poland
Email: sklep@vest-pol.pl
Phone: 731757737

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KQW1F6YSTP7Z0VA6KS2CJQJ4

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

VPPRODID5605905155570055
VPPRODID5705905155570062
VPPRODID5805905155570079
VPPRODID5905905155570031
VPPRODID6005905155570048
VPPRODID6105905155570024