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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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Biokémiai táptalaj flakonban — 6 UDI-DI variants, IVDR (Biolab Zrt)

MD Atlas
Biolab Zrt

Data from EUDAMED, last updated May 24, 2026

Biokémiai táptalaj flakonban

5996650BIOK30004T

6 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: Biolab Zrt

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 5996650BIOK30004T
Device name: Biokémiai táptalaj flakonban
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Mar 17, 2023

Manufacturer & authorised representative

Manufacturer

Name: Biolab Zrt
SRN: HU-MF-000024675
Country: Hungary
Email: mir@biolab.hu

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GVQBKS1Y680SC5HQVQD6THMX

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

Acetate Differential Agar (100 ml)05996650003094
Acetate Differential Agar (250 ml)05996650003100
Acetate Differential Agar (500 ml)05996650003117
Triple Sugar Iron (TSI) Agar, PH EUR (100 ml)05996650003155
Triple Sugar Iron (TSI) Agar, PH EUR (250 ml)05996650003162
Triple Sugar Iron (TSI) Agar, PH EUR (500 ml)05996650003179