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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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Fyziologický roztok — 17 UDI-DI variants, IVDR (LabMediaServis s.r.o.)

MD Atlas
LabMediaServis s.r.o.

Data from EUDAMED, last updated May 23, 2026

Fyziologický roztok

85942104700000000FREU

17 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: LabMediaServis s.r.o.

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 85942104700000000FREU
Device name: Fyziologický roztok
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: LabMediaServis s.r.o.
SRN: CZ-MF-000045078
Country: Czechia
Email: info@labmediaservis.cz

Variants by status

UDI-DI variants

17 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KP37B0DNSF1CSRTJR2XCP7A0

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

FR500008594210470651
FR3,508594210470590
FR4MP08594210472259
FR3MP08594210472273
FR1MP08594210472297
FR100008594210470569
FR208594210470576
FR908594210470620
FR3,5MP08594210472266
FR408594210470606
FRC1908594210470545
FR108594210470552
FR308594210470583
FR2MP08594210472280
FR50008594210470644
FR1008594210470637
FR508594210470613