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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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Kompresy z netkaného textilu nesterilné — 3 UDI-DI variants, MDR

MD Atlas
VIDRA a spol. s.r.o.

Data from EUDAMED, last updated May 31, 2026

Kompresy z netkaného textilu nesterilné

858800101040005GN

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: VIDRA a spol. s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 858800101040005GN
Device name: Kompresy z netkaného textilu nesterilné
Device model: Kompresy z netkaného textilu nesterilné
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: VIDRA a spol. s.r.o.
SRN: SK-MF-000005837
Country: Slovakia
Email: info@vidra.sk
Phone: +421 41 507 10 10

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KSJXSZPSQABWPJBER1X89HPR

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

10104000508588003855121
10104000708588003855145
10104000608588003855138