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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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Transport medium for PCR swabs — 2 UDI-DI variants, IVDR

MD Atlas
Immundiagnostik AG

Data from EUDAMED, last updated May 23, 2026

Transport medium for PCR swabs

4050598IASwabMedC2

2 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: Immundiagnostik AG

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Device characteristics

Reagent

Identity & classification

Basic UDI-DI: 4050598IASwabMedC2
Device name: Transport medium for PCR swabs
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jul 1, 2022

Manufacturer & authorised representative

Manufacturer

Name: Immundiagnostik AG
SRN: DE-MF-000020905
Country: Germany
Email: info@immundiagnostik.com
Phone: +496251701900

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G6WX8P1J1RZTP0416HWTR3PY

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

Transport medium for PCR swabs, tubes. 25 Itr04050598009684
Transport medium for PCR swabs, tubes. 25 Itr, blue04050598009677