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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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Poduszka — 3 UDI-DI variants, MDR

MD Atlas
"JOHN COTTON EUROPE" SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

Data from EUDAMED, last updated May 31, 2026

Poduszka

5905428PEC14M

3 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: "JOHN COTTON EUROPE" SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5905428PEC14M
Device name: Poduszka
Device model: PEC 1
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: "JOHN COTTON EUROPE" SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ
SRN: PL-MF-000027273
Country: Poland
Email: orders@johncotton.eu

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01K7MJYNXN4FMHTY4TG1WNPHAH

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

PEC 105905428045839
PEC 105905428044917
PEC 105905428044924