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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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Vizeletgyűjtők — 6 UDI-DI variants, IVDR (Biolab Zrt)

MD Atlas
Biolab Zrt

Data from EUDAMED, last updated May 24, 2026

Vizeletgyűjtők

5996650URC90008X

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

Professional testing

Identity & classification

Basic UDI-DI: 5996650URC90008X
Device name: Vizeletgyűjtők
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Feb 18, 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

basicUdiUlid01GSHYT6VC6ZPTDMFWJNBY2XVH

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

Urine container, 125 ml, non-sterile05996650001403
Urine container, 200 ml, non-sterile05996650001489
Urine container, 60 ml, non-sterile05996650001441
URC9000505996650001380
URC9001105996650001465
URC9000705996650001427