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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, sterilní — 58 UDI-DI variants, MDR (STERIWUND spol. s r.o.)

MD Atlas
STERIWUND spol. s r.o.

Data from EUDAMED, last updated May 23, 2026

Kompres, sterilní

859515411KOMPRES36

58 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: STERIWUND spol. s r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 859515411KOMPRES36
Device name: Kompres, sterilní
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: STERIWUND spol. s r.o.
SRN: CZ-MF-000036963
Country: Czechia
Email: steriwund@steriwund.cz
Phone: +420 733 110 862

Variants by status

UDI-DI variants

58 UDI-DI variants

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Applied filters

basicUdiUlid01KJ5NRF4DMN9VQ1SZ4A9MFR0V

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

Non-woven swab, sterile08595154101410
Non-woven swab, sterile08595154101953
Non-woven swab, sterile08595154101250
Non-woven swab, sterile08595154115721
Non-woven swab, sterile08595154101656
Non-woven swab, sterile08595154114755
Non-woven swab, sterile08595154101748
Non-woven swab, sterile08595154101816

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