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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

004 — IVDR Class A IVDR by Zdravotní ústav se…

MD Atlas
Zdravotní ústav se sídlem v Ostravě

EUDAMED last updated this device on May 24, 2025

004

08594224840037T2

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: 08594224840037
Reference / catalog number: 004

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Manufacturer information

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

Related devices

01385942248401299ROn the market 01885942248401749WOn the market 00208594224840013SLOn the market 00308594224840020SHOn the market 01985942248401819TOn the market

Market distribution

Primary placement in Czechia; available across 1 country total.

Placed on the market in Czechia; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08594224840037
Basic UDI-DI: 08594224840037T2
Reference / catalog number: 004
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: 20
Additional product description: KA=Columbia krevní agar + 5 % ovčí krve se používá jako médium pro kultivaci všech typů vzorků. Přítomnost krve umožňuje prokázat hemolytické vlastnosti určitých kmenů bakterií.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0104010499PREPARED MEDIA IN PLATES - OTHER

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

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Manufacturing date
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Software identification

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.