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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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Kompres żelowy — 12 UDI-DI variants, MDR (RESMED Jolanta Sosna)

MD Atlas
RESMED Jolanta Sosna

Data from EUDAMED, last updated May 30, 2026

Kompres żelowy

902768kompres4R

12 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: RESMED Jolanta Sosna

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 902768kompres4R
Device name: Kompres żelowy
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 2, 2023

Manufacturer & authorised representative

Manufacturer

Name: RESMED Jolanta Sosna
SRN: PL-MF-000004329
Country: Poland
Email: info@resmed.com.pl
Phone: 607530601

Variants by status

UDI-DI variants

12 UDI-DI variants

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Applied filters

basicUdiUlid01GTGZH177Y7A6RA72S04MAH5P

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

---05902768109016
---05902768109023
---05902768109047
---05902768109030
---05902768109061
---05902768109054
---05902768109139
---05902768109085
---05902768109108
---05902768109122
---05902768109078
---05902768109009