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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

Medical Source Bridge ZMP07 — Class IIb MDR by MZ Liberec, a.s.

MD Atlas
MZ Liberec, a.s.

EUDAMED last updated this device on May 22, 2026

Medical Source Bridge ZMP07

8596463701ZMPPC

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MZ Liberec, a.s.
UDI-DI code: 08596463002863
Reference / catalog number: ZMP07

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View device family (Basic UDI)

Manufacturer information

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

Critical warnings

No critical warnings reported for this device.

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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: Medical Source Bridge ZMP07
UDI-DI code: 08596463002863
Basic UDI-DI: 8596463701ZMPPC
Reference / catalog number: ZMP07
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: Medgas Power Supply Units are intended for termination of both compressed medical gas and vacuum distribution systems, enabling the safe and functional connection and disconnection of the relevant probes of low-pressure hose assemblies 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, ensuring the safety and effectiveness of medical devices in healthcare facilities. Medgas Power Supply Units are used to connect and support 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.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08596463002863

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

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

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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.