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Organization name
UDI-DI code
Reference / catalog number

OK07-28 — Class IIb MDR by MZ Liberec, a.s.

MD Atlas
MZ Liberec, a.s.

EUDAMED last updated this device on May 21, 2026

OK07-28

8596463702OKSU

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MZ Liberec, a.s.
UDI-DI code: 08596463002733
Reference / catalog number: OK07-28

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Manufacturer information

Organization name: MZ Liberec, a.s.
SRN: CZ-MF-000006120
Manufacturer status: Active

Market distribution

Primary placement in Czechia; available across 1 country total.

Country	On market since	Until
CzechiaPrimary placement	Jan 1, 2007	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08596463002733
Basic UDI-DI: 8596463702OKSU
Reference / catalog number: OK07-28
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Adjustable medgas power supply units are intended for termination of both compressed medical gas and vacuum distribution systems, enabling safe and functional connection and disconnection of the relevant probes of low-pressure hose assemblies carried out by the operator while complying with the requirement to ensure specificity for a particular gas, and for termination of electrical and data distribution systems built into profiles suspended on variously arranged spatially adjustable arm assemblies, ensuring the safety and effectiveness of medical devices. Adjustable medgas power supply units are used for connection and carrying of other medical devices and additional equipment intended for the prevention, treatment or alleviation of disease.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z120309MEDICAL/MEDICINAL GAS PIPELINE SYSTEMS AND RELATED ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

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.