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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

027 — 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

027

08594224840266TK

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: 08594224840266
Reference / catalog number: 027

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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: 08594224840266
Basic UDI-DI: 08594224840266TK
Reference / catalog number: 027
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: NACL = Slaný Mueller – Hinton agar je standardizované pevné médium doporučené k izolaci mannitolpozitivních stafylokoků, především Staphylococcus aureus
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
Expiration date
Manufacturing date
Serial number
Software identification

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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.