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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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Selenitový bujón — 4 UDI-DI variants, IVDR

MD Atlas
VIAMAR INTERNATIONAL, s.r.o.

Data from EUDAMED, last updated May 23, 2026

Selenitový bujón

85941999298035BU

4 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: VIAMAR INTERNATIONAL, s.r.o.

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Device characteristics

ReagentProfessional testingAnimal tissues / cells

Identity & classification

Basic UDI-DI: 85941999298035BU
Device name: Selenitový bujón
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jan 9, 2026

Manufacturer & authorised representative

Manufacturer

Name: VIAMAR INTERNATIONAL, s.r.o.
SRN: CZ-MF-000038013
Country: Czechia
Email: viamar@volny.cz
Phone: +420 724 784 097

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KEGW9KXTXMKM5BYQWZ839E8C

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

Selenite broth08594199920468
Selenite broth 1000ml08594199922837
Selenite broth 100ml08594199922479
Selenite broth 200 ml08594199920321