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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 pufrovaný — 11 UDI-DI variants, IVDR

MD Atlas
LabMediaServis s.r.o.

Data from EUDAMED, last updated May 23, 2026

Fyziologický roztok pufrovaný

8594210470000000FRPK5

11 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: 8594210470000000FRPK5
Device name: Fyziologický roztok pufrovaný
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

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KP37B2Z4QQ603N1P0EQJ2E9K

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

FRP3MP08594210472242
FRP208594210470699
FRP1008594210470774
FRP808594210470750
FRP508594210470729
FRP308594210470705
FRP608594210470736
FRP708594210470743
FRP408594210470712
FRP908594210470767
FRP108594210470682