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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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Gáza hydrofilná kompres nesterilný — 9 UDI-DI variants, MDR

MD Atlas
WWW.KOMPRESS.SK, s.r.o.

Data from EUDAMED, last updated May 31, 2026

Gáza hydrofilná kompres nesterilný

858602916001494

9 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: WWW.KOMPRESS.SK, s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 858602916001494
Device name: Gáza hydrofilná kompres nesterilný
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: WWW.KOMPRESS.SK, s.r.o.
SRN: SK-MF-000053588
Country: Slovakia
Email: kompress@kompress.sk

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KR3J06ZNWN1NJ2WPE83DRXZB

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

A3150708586029160083
A3150608586029160076
A3150308586029160052
A3150508586029160069
A3150908586029160106
A 3150208586029160045
A3150808586029160090
A3151008586029160007
A3150108586029160038