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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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Organization name
UDI-DI code
Reference / catalog number

019 — IVDR Class A IVDR by Zdravotní ústav se…

MD Atlas
Zdravotní ústav se sídlem v Ostravě

EUDAMED last updated this device on May 16, 2026

019

85942248401819T

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Zdravotní ústav se sídlem v Ostravě
UDI-DI code: 08594224840181
Reference / catalog number: 019

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Manufacturer information

Organization name: Zdravotní ústav se sídlem v Ostravě
SRN: CZ-MF-000046342
Manufacturer status: Active

Market distribution

Primary placement in Czechia; available across 1 country total.

Country	On market since	Until
CzechiaPrimary placement	Jul 1, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08594224840181
Basic UDI-DI: 85942248401819T
Reference / catalog number: 019
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: ENT = Selektivně diagnostická půda k záchytu enterokoků z klinického materiálu
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0104010405NON-CHROMOGENIC MEDIA (PLATES)

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
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Manufacturing date
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Software identification

Related devices

01385942248401299ROn the market 01885942248401749WOn the market 00208594224840013SLOn the market 00308594224840020SHOn the market 0208594224840198ACOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.